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The purpose of this study is to evaluate outcomes following electromagnetic navigation bronchoscopyâ„¢ (ENBâ„¢) procedures using the superDimensionâ„¢ navigation system.
This clinical trial information was submitted voluntarily under the applicable law and, therefore, certain submission deadlines may not apply. (That is, clinical trial information for this applicable clinical trial was submitted under section 402(j)(4)(A) of the Public Health Service Act and 42 CFR 11.60 and is not subject to the deadlines established by sections 402(j)(2) and (3) of the Public Health Service Act or 42 CFR 11.24 and 11.44.)
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Electromagnetic Navigation Bronchoscopy | Procedure |
|
| Measure | Description | Time Frame |
|---|---|---|
| Incidence of Pneumothorax (Grade 2+) | The primary endpoint is the incidence of pneumothorax related to the ENBâ„¢ index procedure rated as Grade 2 or higher according to the Common Terminology Criteria for Adverse Events (CTCAE) scale. Pneumothorax is a disorder characterized by abnormal presence of air in the pleural cavity resulting in the collapse of the lung. Severity increases as grade increases. Grade 1: Asymptomatic; clinical or diagnostic observations only; intervention not indicated; Grade 2: Symptomatic; intervention indicated (e.g., tube placement without sclerosis); Grade 3: Sclerosis and/or operative intervention indicated; hospitalization indicated; Grade 4: Life-threatening consequences; urgent intervention indicated; Grade 5: Death | index procedure visit |
| Measure | Description | Time Frame |
|---|---|---|
| Incidence of Pneumothorax (All) | The incidence of pneumothorax related to all ENBâ„¢ index procedures will be evaluated. | index procedure visit |
| Incidence of Bronchopulmonary Hemorrhage | The incidence of bronchopulmonary hemorrhage (rated as Grade 2 or higher according to th CTCAE scale) related to all ENBâ„¢ index procedures will be evaluated. Bronchopulmonary hemorrhage is a disorder characterized by bleeding from the bronchial wall and/or lung parenchyma. Severity increases as grade increases. Grade 1: Mild symptoms; intervention not indicated; Grade 2: Moderate symptoms; medical intervention indicated; Grade 3: Transfusion, radiologic, endoscopic, or operative intervention indicated (e.g., hemostasis of bleeding site); Grade 4: Life-threatening respiratory or hemodynamic compromise; intubation or urgent intervention indicated; Grade 5: Death |
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Inclusion Criteria:
Exclusion Criteria:
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Subjects that meet the various inclusion/exclusion criteria will be enrolled consecutively by each participating site.
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| Name | Affiliation | Role |
|---|---|---|
| Sandeep Khandhar, MD | Inova Fairfax Hospital | Principal Investigator |
| Erik Folch, MD | Massachusetts General Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Alabama at Birmingham | Birmingham | Alabama | 35294 | United States | ||
| Pulmonary Associates of Mobile, P.C. |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 37717851 | Derived | Sarnaik KS, Linden PA, Gasnick A, Bassiri A, Manyak GA, Jarrett CM, Sinopoli JN, Tapias Vargas L, Towe CW. Computational risk model for predicting 2-year malignancy of pulmonary nodules using demographic and radiographic characteristics. J Thorac Cardiovasc Surg. 2024 Jun;167(6):1910-1924.e2. doi: 10.1016/j.jtcvs.2023.09.027. Epub 2023 Sep 17. | |
| 30958102 |
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| ID | Title | Description |
|---|---|---|
| FG000 | NAVIGATE (Single Arm Study) | Observational NAVIGATE arm (single arm study, no comparator) |
| Title | Milestones | Reasons Not Completed | |||||
|---|---|---|---|---|---|---|---|
| Overall Study |
|
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP_ICF | Yes | Yes | Yes | Study Protocol, Statistical Analysis Plan, and Informed Consent Form | Nov 17, 2015 |
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| index procedure visit |
| Incidence of Respiratory Failure | The incidence of respiratory failure (rated as Grade 4 or higher according to the CTCAE scale) related to all ENBâ„¢ index procedures will be evaluated. A respiratory failure is a disorder characterized by impaired gas exchange by the respiratory system resulting in hypoxemia and a decrease in oxygenation of the tissues that may be associated with an increase in arterial levels of carbon dioxide. Severity increases as grade increases. Within CTCAE, there are no grades 1, 2, or 3 for Respiratory Failure. Grade 4: Life-threatening consequences; urgent intervention, intubation, or ventilatory support indicated; Grade 5: Death | index procedure visit |
| Quality of Life (Mobility, Self-care, Activities, Pain/Discomfort, Anxiety/Depression, Health State) | Subject health status evaluated by EuroQol-5d (EQ-5D) questionnaire at all visits. (Mobility, Self-care, Activities, Pain/Discomfort, Anxiety/Depression, Health state) Questionnaire from EuroQol Group. Outcome reported on overall health state over time. 0 = worst imaginable health state, 100 = best imaginable health state. | Baseline, 1 month, 12 month, and 24 month follow up visits |
| Subject Satisfaction | Subject satisfaction evaluation at the 1 month visit. The question was "overall, how satisfied were you with the ENB procedure". Options were:
| at the 1 month follow up visit |
| Subject Productivity and Activity | Electromagnetic Navigation Bronchoscopy (ENB) procedure effect on subject productivity and activity using the ENB Productivity and Activity Questionnaire (ENB-PAQ) will be evaluated. The outcome measurement is the effect of ENB on their regular daily activities on a scale of 0-10 (0=no effect, 10=completely prevented). | at the 1 month follow up visit |
| Diagnostic Yield | Diagnostic yield will be evaluated for all ENBâ„¢ index procedures performed for suspicion of cancer or other lung diseases in a lung lesion. Diagnostic yield was calculated per subject as the rate of true positives (TP) (for malignancy) plus true negatives (TN) (for malignancy) out of all subjects with attempted lung lesion biopsies (the denominator included subjects with no tissue obtained due to unsuccessful navigation). | up to 24 months |
| Sensitivity | Sensitivity will be evaluated for all ENBâ„¢ index procedures performed for suspicion of cancer or other lung diseases in a lung lesion. [True Positives =TP, False Negatives = FN]. (TP / [TP+FN]) | up to 24 months |
| Specificity | Specificity will be evaluated for all ENBâ„¢ index procedures performed for suspicion of cancer or other diseases in a lung lesion. [True Negatives = TN, False Positives = FN] (TN / [FP+TN]) | up to 24 months |
| Positive Predictive Value | Positive predictive value (PPV) will be evaluated for all ENBâ„¢ index procedures performed for suspicion of cancer or other diseases in a lung lesion. [True Positives = TP, False Positives = FP] (TP / [TP+FP]) | up to 24 months |
| Negative Predictive Value | Negative Predictive Value (NPV) will be evaluated for all ENBâ„¢ index procedures performed for suspicion of cancer or other diseases in a lung lesion. [True Negatives = TN, False Negatives = FN] (TN / [FN+TN]) | up to 24 months |
| Repeat Biopsy Rate | Repeat biopsy rate due to lack of diagnosis during the ENBâ„¢ index procedure will be evaluated for all ENBâ„¢ index procedures performed for suspicion of cancer or other diseases in a lung lesion. | up to 24 months |
| Tissue Adequacy for Molecular Genetic Testing | Tissue adequacy for molecular genetic testing (if applicable). | at index procedure visit |
| Diagnosis | Diagnosis will be evaluated for all ENBâ„¢ index procedures performed for suspicion of cancer or other diseases in a lung lesion (per subject) | up to 24 months |
| Stage at Diagnosis | Stage at diagnosis (if applicable) will be evaluated for all ENBâ„¢ index procedures performed for suspicion of cancer or other diseases in a lung lesion. (Diagnosis worsens as stage number increases). Refer to the American Joint Committee on Cancer, 7th edition on Lung Cancer Staging. A brief description is provided here. Stage I = small lesions, no lymph node involvement Stage II = larger lesions and/or lymph nodes on sides of lung involved Stage III = larger lesions and/or lymph nodes in middle of chest involved Stage IV = metastases to other organs | up to 24 months |
| Success Rate of Accurate Placement of Fiducial Markers | The success rate of accurate placement of fiducial markers demonstrated through follow up imaging will be evaluated for all ENBâ„¢ index procedures conducted for placement of fiducial markers. | at index procedure visit |
| Success Rate of Dye Marking | The success rate of dye marking demonstrated by successful surgical resection will be evaluated for all ENBâ„¢ index procedures conducted for dye marking in preparation for surgical resection. | at index procedure visit |
| Success Rate of Obtaining Lymph Node Biopsy | The success rate of obtaining a lymph node biopsy to provide the stage of diagnosis will be evaluated for all ENBâ„¢ index procedures conducted for a lymph node biopsy. | at index procedure visit |
| Mobile |
| Alabama |
| 35294 |
| United States |
| Palo Alto Medical Foundation | Mountain View | California | 94040 | United States |
| Pulmonary and Sleep of Tampa Bay | Brandon | Florida | 33511 | United States |
| Ocala Lung and Critical Care | Ocala | Florida | 34471 | United States |
| Cancer Treatment Centers of America | Newnan | Georgia | 30265 | United States |
| The University of Chicago | Chicago | Illinois | 60637 | United States |
| Pulmonary and Critical Care Associates of Baltimore | Baltimore | Maryland | 21237 | United States |
| University of Michigan Health Systems | Ann Arbor | Michigan | 48109 | United States |
| Virtua Medical Group, PA | Marlton | New Jersey | 08053 | United States |
| University of Rochester | Rochester | New York | 14627 | United States |
| Carolina's Healthcare System | Charlotte | North Carolina | 28207 | United States |
| Duke University | Durham | North Carolina | 27705 | United States |
| East Carolina University | Greenville | North Carolina | 27834 | United States |
| Pinehurst Medical Center | Pinehurst | North Carolina | 28374 | United States |
| University of Cincinnati Physicians Company LLC | Cincinnati | Ohio | 45206 | United States |
| University Hospitals of Case Medical Center | Cleveland | Ohio | 44106 | United States |
| Cleveland Clinic | Cleveland | Ohio | 44195 | United States |
| Penn Highlands Healthcare | DuBois | Pennsylvania | 15801 | United States |
| UPMC - Shadyside Medical Center | Pittsburgh | Pennsylvania | 15232 | United States |
| Pulmonary Medicine Center of Chattanooga - Memorial Health | Chattanooga | Tennessee | 37404 | United States |
| Blount Memorial Hospital | Maryville | Tennessee | 37804 | United States |
| Vanderbilt University | Nashville | Tennessee | 37235 | United States |
| Seton Medical Center Austin | Austin | Texas | 78701 | United States |
| East Texas Medical Center | Tyler | Texas | 75701 | United States |
| Providence Health Center | Waco | Texas | 76712 | United States |
| Inova Fairfax Hospital | Falls Church | Virginia | 22042 | United States |
| Charleston Area Medical Center | Charleston | West Virginia | 25304 | United States |
| Gundersen Lutheran Medical Foundation, Inc | La Crosse | Wisconsin | 54601 | United States |
| AKH Linz | Linz | 4020 | Austria |
| Salzburger Landesklinik (SALK) | Salzburg | Austria |
| Rigshospitalet - Copenhagen | Copenhagen | Denmark |
| University Hospitals of Saint Etienne France | Saint-Etienne | France |
| Azienda Ospedaliero Universitaria Careggi | Florence | Italy |
| IRCCS Azienda Ospedaliera Universitaria San Martino - IST | Genova | 16132 | Italy |
| Hospital Fundacion Jimenez Diaz | Madrid | Spain |
| St. Bartholomew's Hospital | London | United Kingdom |
| Bowling MR, Folch EE, Khandhar SJ, Kazakov J, Krimsky WS, LeMense GP, Linden PA, Murillo BA, Nead MA, Pritchett MA, Teba CV, Towe CW, Williams T, Anciano CJ. Fiducial marker placement with electromagnetic navigation bronchoscopy: a subgroup analysis of the prospective, multicenter NAVIGATE study. Ther Adv Respir Dis. 2019 Jan-Dec;13:1753466619841234. doi: 10.1177/1753466619841234. |
| 28399830 | Derived | Khandhar SJ, Bowling MR, Flandes J, Gildea TR, Hood KL, Krimsky WS, Minnich DJ, Murgu SD, Pritchett M, Toloza EM, Wahidi MM, Wolvers JJ, Folch EE; NAVIGATE Study Investigators. Electromagnetic navigation bronchoscopy to access lung lesions in 1,000 subjects: first results of the prospective, multicenter NAVIGATE study. BMC Pulm Med. 2017 Apr 11;17(1):59. doi: 10.1186/s12890-017-0403-9. |
| 27113209 | Derived | Folch EE, Bowling MR, Gildea TR, Hood KL, Murgu SD, Toloza EM, Wahidi MM, Williams T, Khandhar SJ. Design of a prospective, multicenter, global, cohort study of electromagnetic navigation bronchoscopy. BMC Pulm Med. 2016 Apr 26;16(1):60. doi: 10.1186/s12890-016-0228-y. |
| Procedure |
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| 1-Month |
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| 12-Month |
|
| 24-Month |
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| COMPLETED |
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| NOT COMPLETED |
|
|
1388 subjects were enrolled. 1329 subjects had an indication for procedure for lesion biopsy. 1260 subjects had procedure for biopsy with successful navigation. 1529 is the number of lesions for biopsy.
| ID | Title | Description |
|---|---|---|
| BG000 | NAVIGATE (Single Arm Study) | Observational NAVIGATE arm (single arm study, no comparator) |
| Units | Counts |
|---|---|
| Participants |
|
| Number of Lesions for Biopsy |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes | ||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Age, Categorical | Count of Participants | Participants | Participants |
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| Age, Continuous | Mean | Standard Deviation | years | Participants |
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| Sex: Female, Male | Count of Participants | Participants | Participants |
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| Ethnicity (NIH/OMB) | Count of Participants | Participants | Participants |
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| Race/Ethnicity, Customized | Count of Participants | Participants | Participants |
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| Region of Enrollment | Number | participants | Participants |
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| Tobacco history (current or former) | Count of Participants | Participants | Participants |
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| Chronic obstructive pulmonary disease | Count of Participants | Participants | Participants |
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| Personal history of cancer | Count of Participants | Participants | Participants |
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| Family history of cancer | Count of Participants | Participants | Participants |
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| General anesthesia | Count of Participants | Participants | Participants |
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| Radial Endobronchial Ultrasound (R-EBUS) used during Electromagnetic Navigation Bronchoscopy (ENB) | Count of Participants | Participants | Participants |
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| Cone-beam Computed Tomography (CBCT) used during ENB | Count of Participants | Participants | Participants |
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| Fluoroscopy used during ENB | Number of lesions (subjects could have more than one lesion) | Number | number of lesions | Number of Lesions for Biopsy |
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| Rapid on-site evaluation (ROSE) used | Number of subjects undergoing ENB for lesion biopsy where navigation was successful | Count of Participants | Participants | Participants |
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| Average number of lesions biopsied per subject | 1329 subjects who underwent ENB for lung lesion biopsy | Mean | Standard Deviation | Number of lesions | Participants |
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| ||||||||||||||||||||||
| Lesion size (mm) | There were 1529 lesions in the study. 1528 reported measurement on lesion size. | Number of lesions where size was provided | Median | Inter-Quartile Range | millimeters | Number of Lesions for Biopsy |
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| Upper lobe lesion location | Number of lesions (subjects could have more than one lesion) | Number | number of lesions | Number of Lesions for Biopsy |
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| Peripheral third of the lung | Number of lesions (subjects could have more than one lesion) | Number | number of lesions | Number of Lesions for Biopsy |
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| Lesion distance to pleura (mm) | Number of lesions where distance was provided. 1514 lesions in 1317 subjects had "lesion distance to pleura" information. | Median | Inter-Quartile Range | millimeters | Number of Lesions for Biopsy |
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| Pure to mostly ground glass opacity (GGO) lesions (Suzuki Class 1 or 2) | Number of lesions where ground glass was evaluated. 1523 lesions in 1323 subjects where ground glass opacity (GGO) was evaluated. | Number | participants | Number of Lesions for Biopsy |
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| Spiculated lesion border | Number of lesions where lesion border was evaluated and reported. 1527 lesions in 1328 subjects had lesion border information. | Number | participants | Number of Lesions for Biopsy |
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| Bronchus sign present on Computed Tomography (CT) | Number of lesions where bronchus sign presence was evaluated | Number | participants | Number of Lesions for Biopsy |
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| Pre-test probability of malignancy >65% (Physician Estimate) | Number of lesions where the physicians estimate of pre-test probability of malignancy was evaluated | Number | number of lesions | Number of Lesions for Biopsy |
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| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | ||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Incidence of Pneumothorax (Grade 2+) | The primary endpoint is the incidence of pneumothorax related to the ENBâ„¢ index procedure rated as Grade 2 or higher according to the Common Terminology Criteria for Adverse Events (CTCAE) scale. Pneumothorax is a disorder characterized by abnormal presence of air in the pleural cavity resulting in the collapse of the lung. Severity increases as grade increases. Grade 1: Asymptomatic; clinical or diagnostic observations only; intervention not indicated; Grade 2: Symptomatic; intervention indicated (e.g., tube placement without sclerosis); Grade 3: Sclerosis and/or operative intervention indicated; hospitalization indicated; Grade 4: Life-threatening consequences; urgent intervention indicated; Grade 5: Death | All subjects included in this analysis | Posted | Count of Participants | Participants | index procedure visit |
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| Secondary | Incidence of Pneumothorax (All) | The incidence of pneumothorax related to all ENBâ„¢ index procedures will be evaluated. | Posted | Count of Participants | Participants | index procedure visit |
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| Secondary | Incidence of Bronchopulmonary Hemorrhage | The incidence of bronchopulmonary hemorrhage (rated as Grade 2 or higher according to th CTCAE scale) related to all ENBâ„¢ index procedures will be evaluated. Bronchopulmonary hemorrhage is a disorder characterized by bleeding from the bronchial wall and/or lung parenchyma. Severity increases as grade increases. Grade 1: Mild symptoms; intervention not indicated; Grade 2: Moderate symptoms; medical intervention indicated; Grade 3: Transfusion, radiologic, endoscopic, or operative intervention indicated (e.g., hemostasis of bleeding site); Grade 4: Life-threatening respiratory or hemodynamic compromise; intubation or urgent intervention indicated; Grade 5: Death | Posted | Count of Participants | Participants | index procedure visit |
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| Secondary | Incidence of Respiratory Failure | The incidence of respiratory failure (rated as Grade 4 or higher according to the CTCAE scale) related to all ENBâ„¢ index procedures will be evaluated. A respiratory failure is a disorder characterized by impaired gas exchange by the respiratory system resulting in hypoxemia and a decrease in oxygenation of the tissues that may be associated with an increase in arterial levels of carbon dioxide. Severity increases as grade increases. Within CTCAE, there are no grades 1, 2, or 3 for Respiratory Failure. Grade 4: Life-threatening consequences; urgent intervention, intubation, or ventilatory support indicated; Grade 5: Death | Posted | Count of Participants | Participants | index procedure visit |
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| Secondary | Quality of Life (Mobility, Self-care, Activities, Pain/Discomfort, Anxiety/Depression, Health State) | Subject health status evaluated by EuroQol-5d (EQ-5D) questionnaire at all visits. (Mobility, Self-care, Activities, Pain/Discomfort, Anxiety/Depression, Health state) Questionnaire from EuroQol Group. Outcome reported on overall health state over time. 0 = worst imaginable health state, 100 = best imaginable health state. | Number of subjects who completed the EQ-5D at the baseline visit. | Posted | Mean | Standard Deviation | score on a scale | Baseline, 1 month, 12 month, and 24 month follow up visits |
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| Secondary | Subject Satisfaction | Subject satisfaction evaluation at the 1 month visit. The question was "overall, how satisfied were you with the ENB procedure". Options were:
| Subjects who completed the 1-month subject satisfaction questionnaire (How satisfied are you with ENB on a scale of 1-5) | Posted | Mean | Standard Deviation | score on a scale | at the 1 month follow up visit |
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| Secondary | Subject Productivity and Activity | Electromagnetic Navigation Bronchoscopy (ENB) procedure effect on subject productivity and activity using the ENB Productivity and Activity Questionnaire (ENB-PAQ) will be evaluated. The outcome measurement is the effect of ENB on their regular daily activities on a scale of 0-10 (0=no effect, 10=completely prevented). | Number of subjects who completed the ENB-PAQ at 1-month | Posted | Mean | Standard Deviation | score on a scale | at the 1 month follow up visit |
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| Secondary | Diagnostic Yield | Diagnostic yield will be evaluated for all ENBâ„¢ index procedures performed for suspicion of cancer or other lung diseases in a lung lesion. Diagnostic yield was calculated per subject as the rate of true positives (TP) (for malignancy) plus true negatives (TN) (for malignancy) out of all subjects with attempted lung lesion biopsies (the denominator included subjects with no tissue obtained due to unsuccessful navigation). | Per subject including all those with attempted lung lesion biopsies. This includes any with unsuccessful navigation, but excludes subjects with insufficient follow-up where True Positive, True Negative, False Positive and False Negative could not be determined by 24 months. | Posted | Count of Participants | Participants | up to 24 months |
|
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| Secondary | Sensitivity | Sensitivity will be evaluated for all ENBâ„¢ index procedures performed for suspicion of cancer or other lung diseases in a lung lesion. [True Positives =TP, False Negatives = FN]. (TP / [TP+FN]) | Number of subjects with a True Positive (TP) for Malignancy or False Negative (FN) for Malignancy diagnosis by 24-months. | Posted | Count of Participants | Participants | up to 24 months |
|
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| Secondary | Specificity | Specificity will be evaluated for all ENBâ„¢ index procedures performed for suspicion of cancer or other diseases in a lung lesion. [True Negatives = TN, False Positives = FN] (TN / [FP+TN]) | Number of subjects with a False Positive (FP) for Malignancy or True Negative (TN) for Malignancy diagnosis by 24-months. | Posted | Count of Participants | Participants | up to 24 months |
|
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| Secondary | Positive Predictive Value | Positive predictive value (PPV) will be evaluated for all ENBâ„¢ index procedures performed for suspicion of cancer or other diseases in a lung lesion. [True Positives = TP, False Positives = FP] (TP / [TP+FP]) | Number of subjects with a True Positive (TP) for Malignancy or False Positive (FP) for Malignancy diagnosis by 24-months. | Posted | Count of Participants | Participants | up to 24 months |
|
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| Secondary | Negative Predictive Value | Negative Predictive Value (NPV) will be evaluated for all ENBâ„¢ index procedures performed for suspicion of cancer or other diseases in a lung lesion. [True Negatives = TN, False Negatives = FN] (TN / [FN+TN]) | Number of subjects with a False Negative (FN) for Malignancy or True Negative (TN) for Malignancy diagnosis by 24-months. | Posted | Count of Participants | Participants | up to 24 months |
|
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| Secondary | Repeat Biopsy Rate | Repeat biopsy rate due to lack of diagnosis during the ENBâ„¢ index procedure will be evaluated for all ENBâ„¢ index procedures performed for suspicion of cancer or other diseases in a lung lesion. | Number of subjects with navigation complete and tissue obtained | Posted | Count of Participants | Participants | up to 24 months |
|
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| Secondary | Tissue Adequacy for Molecular Genetic Testing | Tissue adequacy for molecular genetic testing (if applicable). | This is the number of lesions diagnosed with primary lung adenocarcinoma or non-small-cell lung cancer not otherwise specified, where molecular genetic testing was attempted. This does not include all lesions biopsied as not all lesions had one of these specific diagnoses, nor did all these with these specific diagnoses have molecular testing attempted. | Posted | Count of Units | Lesions | at index procedure visit | Lesions | Lesions |
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| Secondary | Diagnosis | Diagnosis will be evaluated for all ENBâ„¢ index procedures performed for suspicion of cancer or other diseases in a lung lesion (per subject) | Number of subjects where navigation was complete and tissue was obtained for a diagnosis. Subjects with multiple lesion diagnoses may be represented more than once in all subcategories. | Posted | Count of Units | Diagnoses | No | up to 24 months | Diagnoses | Diagnoses |
|
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| Secondary | Stage at Diagnosis | Stage at diagnosis (if applicable) will be evaluated for all ENBâ„¢ index procedures performed for suspicion of cancer or other diseases in a lung lesion. (Diagnosis worsens as stage number increases). Refer to the American Joint Committee on Cancer, 7th edition on Lung Cancer Staging. A brief description is provided here. Stage I = small lesions, no lymph node involvement Stage II = larger lesions and/or lymph nodes on sides of lung involved Stage III = larger lesions and/or lymph nodes in middle of chest involved Stage IV = metastases to other organs | Number of subjects diagnosed with primary lung cancer. | Posted | Count of Participants | Participants | up to 24 months |
|
| |||||||||||||||||||||||||||
| Secondary | Success Rate of Accurate Placement of Fiducial Markers | The success rate of accurate placement of fiducial markers demonstrated through follow up imaging will be evaluated for all ENBâ„¢ index procedures conducted for placement of fiducial markers. | Number of subjects where ENB was used to aid in placement of fiducial markers, and follow-up imaging data was available. | Posted | Count of Participants | Participants | at index procedure visit |
|
| |||||||||||||||||||||||||||
| Secondary | Success Rate of Dye Marking | The success rate of dye marking demonstrated by successful surgical resection will be evaluated for all ENBâ„¢ index procedures conducted for dye marking in preparation for surgical resection. | Number of subjects where ENB was used to aid in pleural dye marking. | Posted | Count of Participants | Participants | at index procedure visit |
|
| |||||||||||||||||||||||||||
| Secondary | Success Rate of Obtaining Lymph Node Biopsy | The success rate of obtaining a lymph node biopsy to provide the stage of diagnosis will be evaluated for all ENBâ„¢ index procedures conducted for a lymph node biopsy. | Number of subjects where ENB was used to aid in lymph node biopsy. | Posted | Count of Participants | Participants | at index procedure visit |
|
|
Up to 24 months post procedure
ISO 14155 event definitions were used. The following AEs were required to be reported:
All AEs related to the superDimensionâ„¢ navigation system, associated tools, or ENBâ„¢ procedure (both index and any subsequent repeat ENBâ„¢ procedure); All deaths (all-cause); All pneumothoraces (all-cause); All bronchopulmonary hemorrhages (all-cause); All respiratory failures (all cause) Important note: not all events reported in the study were related to the study procedure or study device.
Not provided
| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | NAVIGATE (Single Arm Study) | Observational NAVIGATE arm (single arm study, no comparator) | 403 | 1,388 | 497 | 1,388 | 96 | 1,388 |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Thrombocytopenia | Blood and lymphatic system disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Acute myocardial infarction | Cardiac disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Cardiac arrest | Cardiac disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Cardiac failure | Cardiac disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Cardiac failure congestive | Cardiac disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Cardio-respiratory arrest | Cardiac disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Cardiopulmonary failure | Cardiac disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Cor pulmonale acute | Cardiac disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Left ventricular failure | Cardiac disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Myocardial infarction | Cardiac disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Gastrointestinal haemorrhage | Gastrointestinal disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Inguinal hernia | Gastrointestinal disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Intestinal infarction | Gastrointestinal disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Intestinal perforation | Gastrointestinal disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Pancreatitis | Gastrointestinal disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Death | General disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Disease progression | General disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Multiple organ dysfunction syndrome | General disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Acute hepatic failure | Hepatobiliary disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Cirrhosis alcoholic | Hepatobiliary disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Hepatorenal syndrome | Hepatobiliary disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Bacteraemia | Infections and infestations | MedDRA 22.0 | Systematic Assessment |
| |
| Bacterial sepsis | Infections and infestations | MedDRA 22.0 | Systematic Assessment |
| |
| Lower respiratory tract infection | Infections and infestations | MedDRA 22.0 | Systematic Assessment |
| |
| Pneumonia | Infections and infestations | MedDRA 22.0 | Systematic Assessment |
| |
| Pneumonia fungal | Infections and infestations | MedDRA 22.0 | Systematic Assessment |
| |
| Sepsis | Infections and infestations | MedDRA 22.0 | Systematic Assessment |
| |
| Septic shock | Infections and infestations | MedDRA 22.0 | Systematic Assessment |
| |
| Transmission of an infectious agent via product | Infections and infestations | MedDRA 22.0 | Systematic Assessment |
| |
| Gun shot wound | Injury, poisoning and procedural complications | MedDRA 22.0 | Systematic Assessment |
| |
| Post procedural haemorrhage | Injury, poisoning and procedural complications | MedDRA 22.0 | Systematic Assessment |
| |
| Procedural pneumothorax | Injury, poisoning and procedural complications | MedDRA 22.0 | Systematic Assessment |
| |
| Failure to thrive | Metabolism and nutrition disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Hyperglycaemia | Metabolism and nutrition disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Acute myeloid leukaemia | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Adenocarcinoma | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Adenocarcinoma of colon | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Adenocarcinoma pancreas | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Brain neoplasm malignant | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Breast cancer | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Breast cancer metastatic | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Breast cancer stage IV | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Bronchial carcinoma | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Cervix carcinoma | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Colon cancer | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Diffuse large B-cell lymphoma | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Extranodal marginal zone B-cell lymphoma (MALT type) | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Invasive ductal breast carcinoma | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Leiomyosarcoma metastatic | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Lung adenocarcinoma | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Lung cancer metastatic | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Lung carcinoma cell type unspecified stage III | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Lung carcinoma cell type unspecified stage IV | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Lung neoplasm malignant | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Lung squamous cell carcinoma metastatic | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Lung squamous cell carcinoma stage IV | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Lymphoma | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Malignant neoplasm progression | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Meningioma malignant | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Metastases to central nervous system | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Metastatic pulmonary embolism | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Metastatic renal cell carcinoma | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Metastatic uterine cancer | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Neoplasm malignant | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Neoplasm progression | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Non-small cell lung cancer | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Non-small cell lung cancer metastatic | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Oesophageal adenocarcinoma | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Oesophageal cancer metastatic | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Pancreatic carcinoma | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Pancreatic carcinoma metastatic | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Pharyngeal cancer | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Prostate cancer | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Rectal cancer | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Renal cancer metastatic | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Renal cell carcinoma | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Small cell lung cancer | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Small cell lung cancer metastatic | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Squamous cell carcinoma | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Squamous cell carcinoma of lung | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Transitional cell carcinoma | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Uterine leiomyosarcoma | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA 22.0 | Systematic Assessment |
| |
| Cerebral infarction | Nervous system disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Cerebrovascular accident | Nervous system disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Goodpasture's syndrome | Renal and urinary disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Renal failure | Renal and urinary disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Acute respiratory failure | Respiratory, thoracic and mediastinal disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Apnoea | Respiratory, thoracic and mediastinal disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Bronchial obstruction | Respiratory, thoracic and mediastinal disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Chronic obstructive pulmonary disease | Respiratory, thoracic and mediastinal disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Haemoptysis | Respiratory, thoracic and mediastinal disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Hypoxia | Respiratory, thoracic and mediastinal disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Interstitial lung disease | Respiratory, thoracic and mediastinal disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Lung disorder | Respiratory, thoracic and mediastinal disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Mediastinal haematoma | Respiratory, thoracic and mediastinal disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Organising pneumonia | Respiratory, thoracic and mediastinal disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Pneumomediastinum | Respiratory, thoracic and mediastinal disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Pneumonia aspiration | Respiratory, thoracic and mediastinal disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Pneumothorax | Respiratory, thoracic and mediastinal disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Pulmonary embolism | Respiratory, thoracic and mediastinal disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Pulmonary haemorrhage | Respiratory, thoracic and mediastinal disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Respiratory failure | Respiratory, thoracic and mediastinal disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Arteriosclerosis | Vascular disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Arteriovenous fistula | Vascular disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Peripheral circulatory failure | Vascular disorders | MedDRA 22.0 | Systematic Assessment |
|
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Pneumothorax | Respiratory, thoracic and mediastinal disorders | MedDRA 22.0 | Systematic Assessment |
| |
| Pulmonary haemorrhage | Respiratory, thoracic and mediastinal disorders | MedDRA 22.0 | Systematic Assessment |
|
Institution and Investigator shall not publish the Study results until after Sponsor's multi-site publication of complete and final study results or until the elapse of twelve (12) months from the close of the Study at all Study sites, whichever occurs earlier; unless approved by Sponsor.
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Jennifer Wolvers | Medtronic | 763-258-9405 | Jennifer.Wolvers@Medtronic.com |
| Feb 5, 2021 |
| Prot_SAP_ICF_000.pdf |
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