Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Class |
|---|---|
| Technische Universität Dresden | OTHER |
Not provided
Not provided
Not provided
Not provided
The results of this study will help to define the capability and reliability of PulmoVista 500 to detect changes in both global and regional ventilation.
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| ICU Patients | Patients currently on or scheduled for ventilator care in the intensive-care-unit (ICU) |
| |
| OLV Patients | Patients scheduled for elective surgery receiving one-lung-ventilation (OLV) |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Lung Monitoring with EIT device (PulmoVista 500) | Device | Patient's lungs will be monitored during clinical routine interventions with Dräger's EIT device (PulmoVista 500). No medical interventions to routine patient care required. |
| Measure | Description | Time Frame |
|---|---|---|
| Monitoring Capabilities of PulmoVista 500 | The cross-correlation between the volume curve of the ventilator and the global impedance curve of PulmoVista 500 was expressed by the cross-correlation coefficient R. The cross-correlation coefficient is a measure to quantify the relationship between the volume curve and the EIT curve. The correlation coefficient R can assume values between [-1, 1] to describe the relationship between the two curves, as is usual for a correlation. To calculate the correlation coefficient, a phase shift between the two curves was taken into account, so the cross-correlation between them was calculated. The phase shift or delay occurs when the signal from the fan is transmitted to the PulmoVista500. The cross-correlation coefficient is determined by calculating the correlation coefficient for the curves within a narrow range of Lags(-15 to 15 ) for each pair of curves and using the maximum value as the value of correlation coefficient (therefore it is called cross-correlation coefficient) | Day 1 |
| Measure | Description | Time Frame |
|---|---|---|
| Detection of Changes in Regional Ventilation | To assess the capability of PulmoVista 500 to detect changes in regional ventilation by evaluating the cross correlation between impedance waveforms derived from PulmoVista 500 and volume curves derived from ventilator during one-lung-ventilation. | Day 1 |
| Assess Changes of Tidal Volumes |
Not provided
Inclusion Criteria
- The population included in the clinical study will be selected from a pool of patients undergoing respiratory support who are scheduled to have their ventilation settings changed.
As a subgroup, patients who are scheduled for surgeries that need one-lung-ventilation (OLV) will be enrolled to the study.
Exclusion Criteria
Not provided
Not provided
Not provided
Intensive care unit (ICU) patients, who are mechanically ventilated via an artificial airway (endotracheal tube or tracheostomy cannula) and who are expected to be subjected to major changes in their ventilator settings will be monitored with the PulmoVista 500 device before, during and after the changes. These changes in the ventilator settings should result in recognizable changes in the distribution of ventilation in the lungs.
AND Patients who are scheduled for surgeries that require blocking of one bronchus
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Peter M Spieth, Prof.Dr. med. | Universitätsklinikum Dresden | Principal Investigator |
| Oliver C Radke, Prof. Dr. | Klinikum Bremerhaven-Reinkenheide gGmbH | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Klinikum Bremerhaven-Reinkenheide gGmbH | Bremerhaven | 27574 | Germany | |||
| Universitätsklinik Dresden |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| ID | Title | Description |
|---|---|---|
| FG000 | ICU Patients | Patients currently on or scheduled for ventilator care in the intensive-care-unit (ICU) Lung Monitoring with EIT device (PulmoVista 500): Patient's lungs will be monitored during clinical routine interventions with Dräger's EIT device (PulmoVista 500). No medical interventions to routine patient care required. |
| FG001 |
| Title | Milestones | Reasons Not Completed | |||||
|---|---|---|---|---|---|---|---|
| Overall Study |
|
Not provided
Not provided
Not provided
| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot | Yes | No | No | Study Protocol | Nov 21, 2016 | Jul 18, 2019 |
Not provided
Not provided
Not provided
Not provided
Assess that changes of tidal volumes induced by ventilator settings can be monitored by the "Trends view" To assess if the changes of tidal volumes induced by ventilator settings can be monitored by the "Trends view", the physician was asked to answer following question of a questionnaire: "Open the view "End-insp. trend" after the PEEP setting has been changed significantly (2 mbar or more). Set C1 at the lower and C2 at the higher PEEP level. Does the image Change: C2 minus C1 and/or the corresponding regional Tidal Variations show the expected redistribution of ventilation from ventral to dorsal?" Possible answers were: "No", "Yes" and "N/A" |
| Day 1 |
| Assess Changes of the End-expiratory Lung Volumes | Assess that changes of the end-expiratory lung volumes (induced by e.g. PEEP changes, recruitment and suctioning maneuvers) can be monitored by "dEELI trend view" To assess if the changes of the end-expiratory lung volumes (induced by e.g. PEEP changes, recruitment and suctioning maneuvers) can be monitored by "dEELI trend view", the physician was asked to answer following two question of a questionnaire: Question 1: "Open the view "dEELI trend" after the PEEP setting has been changed. Set C1 at the lower and C2 at the higher PEEP level. Does the image dEELI: C2 minus C1 show the expected increase of end-exp. lung volume in turquoise (light-blue)?" Question 2: "Open the view "dEELI trend" after lung suction has been conducted. Set C1 at a phase before and C2 during or immediately after the lung suction. Does the image dEELI: C2 minus C1 show the expected decrease of lung volume in orange color?" Possible answers for the both above mentioned questions were "No","Yes" or "N/A2 | Day 1 |
| Safety - Documentation of Any Safety Events | Documentation of any safety events related to the use of PulmoVista 500 | Day 1 |
| Assessing the Use Specific Clinical Helpfulness of PulmoVista 500 by Particular Questionnaire. The Questions Which Were Asked Within the Questionaire Are Listed in the "Outcome Measure Description" | "How easy is it to... Q1: ... identify within the Tidal Image, whether the right and the left lung are evenly ventilated?" Q2: ... quantify the regional ventilation distribution as expressed by the regional Parameters TV ROI 1 - TV ROI 4?" Q3: ... set the cursors to respective positions which allow you to compare ventilation distribution before and after the intervention?" Q4: ... detect increases and/or decreases of regional ventilation?" Q5: ... relate the regional ventilation distribution to and the corresponding parameters from the ventilator, which are displayed in the trend table to each other?" Q7: ... set the cursors to respective positions which allows you assessing lung volume changes induced by the intervention?" Q8: ... detect increases and/or decreases of regional lung volume?" "How useful is the clinical Information on... Q6: ... ventilation redistribution caused by this intervention?" Q9: ... regional lung volume changes caused by this intervention?" | Day 1 |
| Dresden |
| 01307 |
| Germany |
| Medizinische Hochschule Hannover (MHH) | Hanover | 30625 | Germany |
| OLV Patients |
Patients scheduled for elective surgery receiving one-lung-ventilation (OLV) Lung Monitoring with EIT device (PulmoVista 500): Patient's lungs will be monitored during clinical routine interventions with Dräger's EIT device (PulmoVista 500). No medical interventions to routine patient care required. |
| COMPLETED |
|
| NOT COMPLETED |
|
Not provided
| ID | Title | Description |
|---|---|---|
| BG000 | ICU Patients | Patients currently on or scheduled for ventilator care in the intensive-care-unit (ICU) Lung Monitoring with EIT device (PulmoVista 500): Patient's lungs will be monitored during clinical routine interventions with Dräger's EIT device (PulmoVista 500). No medical interventions to routine patient care required. |
| BG001 | OLV Patients | Patients scheduled for elective surgery receiving one-lung-ventilation (OLV) Lung Monitoring with EIT device (PulmoVista 500): Patient's lungs will be monitored during clinical routine interventions with Dräger's EIT device (PulmoVista 500). No medical interventions to routine patient care required. |
| BG002 | Total | Total of all reporting groups |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean | Standard Deviation | years |
| |||||||||||||||
| Sex: Female, Male | Count of Participants | Participants |
| ||||||||||||||||
| Ethnicity (NIH/OMB) | Count of Participants | Participants |
| ||||||||||||||||
| Region of Enrollment | Number | participants |
| ||||||||||||||||
| Height | Mean | Standard Deviation | Centimetre |
| |||||||||||||||
| Weight | Mean | Standard Deviation | kilogram |
| |||||||||||||||
| Body mass index | Mean | Standard Deviation | kg/m^2 |
|
| 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 | Monitoring Capabilities of PulmoVista 500 | The cross-correlation between the volume curve of the ventilator and the global impedance curve of PulmoVista 500 was expressed by the cross-correlation coefficient R. The cross-correlation coefficient is a measure to quantify the relationship between the volume curve and the EIT curve. The correlation coefficient R can assume values between [-1, 1] to describe the relationship between the two curves, as is usual for a correlation. To calculate the correlation coefficient, a phase shift between the two curves was taken into account, so the cross-correlation between them was calculated. The phase shift or delay occurs when the signal from the fan is transmitted to the PulmoVista500. The cross-correlation coefficient is determined by calculating the correlation coefficient for the curves within a narrow range of Lags(-15 to 15 ) for each pair of curves and using the maximum value as the value of correlation coefficient (therefore it is called cross-correlation coefficient) | A Intention-to-Treat (ITT) collective was used as analysis population. The intention-to-treat collective comprises all patients for which both, the impedance waveforms and parallel to them volume waveforms have been generated during ventilation,so that the primary endpoint can be evaluated. | Posted | Mean | Standard Deviation | correlation coefficient | Day 1 |
|
|
| ||||||||||||||||||||||||||||
| Secondary | Detection of Changes in Regional Ventilation | To assess the capability of PulmoVista 500 to detect changes in regional ventilation by evaluating the cross correlation between impedance waveforms derived from PulmoVista 500 and volume curves derived from ventilator during one-lung-ventilation. | For this secondary endpoint the cross-correlation between between impedance waveforms derived from PulmoVista 500 and volume curves derived from Ventilator was calculated only for patients which received one-lung-ventilation (OLV). Therefore no patients from the ICU patients Group were included into the analysis. | Posted | Mean | Standard Deviation | correlation coefficient | Day 1 |
| ||||||||||||||||||||||||||||||
| Secondary | Assess Changes of Tidal Volumes | Assess that changes of tidal volumes induced by ventilator settings can be monitored by the "Trends view" To assess if the changes of tidal volumes induced by ventilator settings can be monitored by the "Trends view", the physician was asked to answer following question of a questionnaire: "Open the view "End-insp. trend" after the PEEP setting has been changed significantly (2 mbar or more). Set C1 at the lower and C2 at the higher PEEP level. Does the image Change: C2 minus C1 and/or the corresponding regional Tidal Variations show the expected redistribution of ventilation from ventral to dorsal?" Possible answers were: "No", "Yes" and "N/A" | This question is only applicable to the patient group of "ICU Patients" as no assessment of the changes of tidal volumes induced by ventilator settings was planned a priori for the "OLV" patient group. | Posted | Count of Participants | Participants | Day 1 |
| |||||||||||||||||||||||||||||||
| Secondary | Assess Changes of the End-expiratory Lung Volumes | Assess that changes of the end-expiratory lung volumes (induced by e.g. PEEP changes, recruitment and suctioning maneuvers) can be monitored by "dEELI trend view" To assess if the changes of the end-expiratory lung volumes (induced by e.g. PEEP changes, recruitment and suctioning maneuvers) can be monitored by "dEELI trend view", the physician was asked to answer following two question of a questionnaire: Question 1: "Open the view "dEELI trend" after the PEEP setting has been changed. Set C1 at the lower and C2 at the higher PEEP level. Does the image dEELI: C2 minus C1 show the expected increase of end-exp. lung volume in turquoise (light-blue)?" Question 2: "Open the view "dEELI trend" after lung suction has been conducted. Set C1 at a phase before and C2 during or immediately after the lung suction. Does the image dEELI: C2 minus C1 show the expected decrease of lung volume in orange color?" Possible answers for the both above mentioned questions were "No","Yes" or "N/A2 | These two questions are only applicable to the patient group of "ICU Patients" as no assessment of the changes of the end-expiratory lung volume was planned a priori within the "OLV" patient group. | Posted | Count of Participants | Participants | Day 1 |
| |||||||||||||||||||||||||||||||
| Secondary | Safety - Documentation of Any Safety Events | Documentation of any safety events related to the use of PulmoVista 500 | Posted | Count of Participants | Participants | Day 1 |
|
| |||||||||||||||||||||||||||||||
| Secondary | Assessing the Use Specific Clinical Helpfulness of PulmoVista 500 by Particular Questionnaire. The Questions Which Were Asked Within the Questionaire Are Listed in the "Outcome Measure Description" | "How easy is it to... Q1: ... identify within the Tidal Image, whether the right and the left lung are evenly ventilated?" Q2: ... quantify the regional ventilation distribution as expressed by the regional Parameters TV ROI 1 - TV ROI 4?" Q3: ... set the cursors to respective positions which allow you to compare ventilation distribution before and after the intervention?" Q4: ... detect increases and/or decreases of regional ventilation?" Q5: ... relate the regional ventilation distribution to and the corresponding parameters from the ventilator, which are displayed in the trend table to each other?" Q7: ... set the cursors to respective positions which allows you assessing lung volume changes induced by the intervention?" Q8: ... detect increases and/or decreases of regional lung volume?" "How useful is the clinical Information on... Q6: ... ventilation redistribution caused by this intervention?" Q9: ... regional lung volume changes caused by this intervention?" | Posted | Count of Participants | Participants | Day 1 |
|
Adverse Event data were collected during the follow-up visit, which takes place once within 1-3 days period after the study day.
Not provided
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 | ICU Patients | Patients currently on or scheduled for ventilator care in the intensive-care-unit (ICU) Lung Monitoring with EIT device (PulmoVista 500): Patient's lungs will be monitored during clinical routine interventions with Dräger's EIT device (PulmoVista 500). No medical interventions to routine patient care required. | 0 | 55 | 7 | 55 | 2 | 55 |
| EG001 | OLV Patients | Patients scheduled for elective surgery receiving one-lung-ventilation (OLV) Lung Monitoring with EIT device (PulmoVista 500): Patient's lungs will be monitored during clinical routine interventions with Dräger's EIT device (PulmoVista 500). No medical interventions to routine patient care required. | 0 | 25 | 1 | 25 | 12 | 25 |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Post procedural swelling | Injury, poisoning and procedural complications | MedDRA (Unspecified) | Systematic Assessment |
| |
| Vascular graft complication | Injury, poisoning and procedural complications | MedDRA 21.0 | Systematic Assessment |
| |
| Respiratory failure | Respiratory, thoracic and mediastinal disorders | MedDRA 21.0 | Systematic Assessment |
| |
| Cardiogenic shock | Cardiac disorders | MedDRA 21.0 | Systematic Assessment |
| |
| Haemodynamic instability | Vascular disorders | MedDRA 21.0 | Systematic Assessment |
| |
| Acute respiratory distress syndrome | Respiratory, thoracic and mediastinal disorders | MedDRA 21.0 | Systematic Assessment |
| |
| Pneumothorax | Respiratory, thoracic and mediastinal disorders | MedDRA 21.0 | Systematic Assessment |
| |
| Intracranial pressure increased | Nervous system disorders | MedDRA 21.0 | Systematic Assessment |
| |
| Cardiac arrest | Cardiac disorders | MedDRA 21.0 | Systematic Assessment |
|
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Procedural pain | Injury, poisoning and procedural complications | MedDRA 21.0 | Systematic Assessment |
| |
| Delirium | Psychiatric disorders | MedDRA 21.0 | Systematic Assessment |
| |
| Hypotension | Vascular disorders | MedDRA 21.0 | Systematic Assessment |
|
Not provided
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Mr. Robin Hüwel | Drägerwerk AG & Co. KGaA | +49 451 882 6830 | ClinicalAffairs@draeger.com |
| Prot_000.pdf |
| SAP | No | Yes | No | Statistical Analysis Plan | Mar 1, 2018 | Jul 18, 2019 | SAP_001.pdf |
| ID | Term |
|---|---|
| D055371 | Acute Lung Injury |
| ID | Term |
|---|---|
| D055370 | Lung Injury |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
Not provided
Not provided
| Male |
|
| Not Hispanic or Latino |
|
| Unknown or Not Reported |
|
| Units | Counts |
|---|---|
| Participants |
|
|
|
|
| OG001 | OLV Patients | Patients scheduled for elective surgery receiving one-lung-ventilation (OLV) Lung Monitoring with EIT device (PulmoVista 500): Patient's lungs will be monitored during clinical routine interventions with Dräger's EIT device (PulmoVista 500). No medical interventions to routine patient care required. |
|
|
|
Patients scheduled for elective surgery receiving one-lung-ventilation (OLV) Lung Monitoring with EIT device (PulmoVista 500): Patient's lungs will be monitored during clinical routine interventions with Dräger's EIT device (PulmoVista 500). No medical interventions to routine patient care required. |
|
|
| 3 |
|
| 4 |
|
| 5 = very easy / very useful |
|
| 3 |
|
| 4 |
|
| 5 = very easy / very useful |
|
| 3 |
|
| 4 |
|
| 5 = very easy / very useful |
|
| 3 |
|
| 4 |
|
| 5 = very easy / very useful |
|
| 3 |
|
| 4 |
|
| 5 = very easy / very useful |
|
| 3 |
|
| 4 |
|
| 5 = very easy / very useful |
|
| 3 |
|
| 4 |
|
| 5 = very easy / very useful |
|
| 3 |
|
| 4 |
|
| 5 = very easy / very useful |
|