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| Name | Class |
|---|---|
| Lucerno Dynamics Limited Liability Company (LLC) | UNKNOWN |
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PET (Positron Emission Tomography) images are used to help make patient management decisions in staging and treatment assessment, often after a cancer diagnosis.
Improper injections of PET tracers (dye) may occur approximately 15% of the time. This is known as extravasation or infiltration, and it compromises the doctor's ability to read the PET image. Often, the site where the tracer is injected into the vein (usually in the inside of the elbow) are not in the images taken, so reading physicians are unaware that an extravasation or infiltration has occurred.
Technology exists to capture time activity curves (amount of tracer in a location over a period of time) during the PET tracer uptake period (usually once the tracer is injected, the tracer circulates for 60 minutes prior to images), which can enable physicians to accurately detect extravasations and infiltration. This information is currently unavailable to physicians reading routine PET/CT (computed tomography) scans.
Time activity curves information gathered from these sensors during the circulation period appear to match the brief pictures taken approximately 70 minutes after the tracer injection.
This study will determine if these time activity curves correspond to PET images of the injection site taken during the tracer uptake period. If time activity curves correspond to PET images, they can be used to determine if the tracer was properly injected. If there was an improper injection, clinicians can be alerted to this fact and interpret the image with this additional information.
PET (Positron Emission Tomography) images are used to help make patient management decisions in staging and treatment assessment, often after a cancer diagnosis.
Improper injections of PET tracers (dye) may occur approximately 15% of the time. This is known as extravasation or infiltration, and it compromises the doctor's ability to read the PET image. Often, the site where the tracer is injected into the vein (usually in the inside of the elbow) are not in the images taken, so reading physicians are unaware that an extravasation or infiltration has occurred.
Technology exists to capture time activity curves (amount of tracer in a location over a period of time) during the PET tracer uptake period (usually once the tracer is injected, the tracer circulates for 60 minutes prior to images), which can enable physicians to accurately detect extravasations. This information is currently unavailable to physicians reading routine PET/CT scans.
Time activity curves information gathered from these sensors during the circulation period appear to match the brief pictures taken approximately 70 minutes after the tracer injection.
This study will determine if these time activity curves correspond to PET images of the injection site taken during the tracer uptake period. If time activity curves correspond to PET images, they can be used to determine if the tracer was properly injected. If there was an improper injection, clinicians can be alerted to this fact and interpret the image with this additional information.
In oncology, whole-body PET/CT is typically performed from the head to the pelvic floor (eyes to thighs). The use of the term whole-body is misleading because the most commonly used field of view (FOV) for arms-up whole-body PET/CT protocols includes only the base of skull to the upper thighs and does not include the brain, skull, and large portions of both upper and lower extremities. In such FOV, the most commonly used site of injection, namely the antecubital fossa (inside of the elbow), is frequently not included in the imaging field. In the Frontiers in Oncology article, Osman also determined that based on the commonly used FOV at most PET/CT centers, that when infiltration is present, it may be unnoticed by clinicians in approximately 31% of the cases.
Lucerno Dynamics, a privately held company in North Carolina, has also discovered that the static image may be incapable of reporting on the quality of FDG administration during the ~60 minute uptake period. Lucerno's system has been used in two investigational studies at two centers. At one center, the system was used with 8 patients for a total of 15 scans. At the other center, the system was used with 40 patients for a total of 85 scans. Similar rates of infiltrations were found to those described in the published articles. Based on this experience, Lucerno has found that infiltrations can partially resolve during the uptake period, so that even if they are visible in the PET image, the image may not reveal the extent of the infiltration. This could severely and negatively impact research and therapy decisions and thus patient outcomes.
The Lucerno devices (Lucerno ID) are nonsignificant risk devices that add only 2-3 minutes to the current standard of care PET/CT scanning process. Lucerno ID sensors are applied to the patient's skin before the injection of the radiotracer and are removed after the FDG uptake period and prior to the PET/CT imaging process. The Lucerno ID has the ability to identify infiltrations, whether they are within or outside the FOV of reviewing clinicians, and can alert clinicians before their patient undergoes a compromised PET/CT scan due to the infiltration. This technology can prevent patients from receiving the additional CT radiation exposure of a compromised scan, can save cost, and can improve patient outcomes by ensuring more accurate PET scan interpretation.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Static Imaging participants | Experimental | This arm of the study assessed participants' static PET/CT images. These were the standard of care images acquired after their standard of care uptake time. These images were assessed visually by a board certified physician and using the Time Activity Curves from the sensor data. Intervention was Lucerno sensors (Lucerno Device Identity Document (LD ID), Lucerno Device 1 (LD1), Lucerno, Lara) placed on participant to monitor radiotracer activity at and around injection site. |
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| Dynamic image participants | Experimental | This arm of the study assessed participants' dynamic PET/CT images. These were the study related images of and around the injection site acquired during the participants' standard of care uptake time. These images were assessed visually by a board certified physician and using the Time Activity Curves from the sensor data. Intervention was Lucerno sensors (LD ID, LD1, Lucerno, Lara) placed on participant to monitor radiotracer activity at and around injection site. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Lucerno ID (identification) System | Device | The Lucerno ID is intended to dynamically measure the uptake of radiotracer in a particular organ or body region during the radiotracer uptake period as part of nuclear medicine (NM) procedures. The Lucerno ID is indicated for use as a tool for trained healthcare professionals (technologists, NM physicians, and radiologists) to help assess whether a radiotracer injection has resulted in an infiltration. The LD ID can be used by healthcare professionals including nuclear medical technologists, nuclear medicine physicians, or any other medical staff in a NM facility, once they have received the necessary training into the use of the system. |
| Measure | Description | Time Frame |
|---|---|---|
| Number of Participants With Intraveneous Infiltration of FDG During Routine PET/CT Imaging by Visually Assessment of Interpreting Physicians | Infiltrations of 18F-2-fluoro-2-deoxy-D-glucose fluorodeoxyglucose (FDG) during Positron Emission Tomography (PET) radiotracer administration can lead to sub-optimal images. We aim to compare rates of radiotracer presence near the injection site detected by physicians. Every subject that participates in an FDG-PET scan received an intervenous injection as part of this study. The number of participants by arm were provided in Static Imaging Participants and Dynamic Imaging Participants. | The time frame would be from the time the sensors were placed to the time the sensors were removed; no more than 2 hours. |
| Measure | Description | Time Frame |
|---|---|---|
| Number of Participants With Lucerno Sensor Device Detected Presence and/or Absence of Intravenous Infiltration | Review collected Lucerno sensor graphical data. The Lucerno time activity curves will capture an amount of activity from the sensors and assess subjects for presence or absence of infiltration at injection site. | The time frame would be from the time the sensors were placed to the time the sensors were removed; no more than 2 hours. |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| SSM Saint Louis University Hospital | St Louis | Missouri | 63104 | United States |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 29127247 | Result | Muzaffar R, Frye SA, McMunn A, Ryan K, Lattanze R, Osman MM. Novel Method to Detect and Characterize 18F-FDG Infiltration at the Injection Site: A Single-Institution Experience. J Nucl Med Technol. 2017 Dec;45(4):267-271. doi: 10.2967/jnmt.117.198408. Epub 2017 Nov 10. | |
| 29042469 | Result | Schaefferkoetter JD, Osman M, Townsend DW. The Importance of Quality Control for Clinical PET Imaging. J Nucl Med Technol. 2017 Dec;45(4):265-266. doi: 10.2967/jnmt.117.198465. Epub 2017 Oct 17. No abstract available. |
| Label | URL |
|---|---|
| Published article: Novel Method to Detect and Characterize 18Fluoride-FDG Infiltration at the Injection Site: A Single-Institution Experience | View source |
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Coded data will be shared with our industry sponsor, Lucerno Dynamics
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| ID | Title | Description |
|---|---|---|
| FG000 | Static Imaging Participants | This arm of the study assessed participants' static Positron Emission Tomography / Computed Tomography (PET/CT) images. These were the standard of care images acquired after their standard of care uptake time. These images were assessed visually by a board certified physician and using the Time Activity Curves from the sensor data. This arm also visually assessed the images at the injection site by a board certified physician. |
| FG001 | Dynamic Image Participants | This arm of the study assessed participants' dynamic Positron Emission Tomography / Computed Tomography (PET/CT) images. These were the study related images of and around the injection site acquired during the participants' standard of care uptake time. These images were assessed visually by a board certified physician and using the Time Activity Curves from the sensor data. This arm also visually assessed the images at the injection site by a board certified physician. |
| Title | Milestones | Reasons Not Completed | ||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
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Data were analyzed by physician review of the static standard of care PET/CT images and dynamic injection site images for visible evidence of radiotracer infiltration. The Time Activity Curves (TACs) generated from the applied sensors were independently assessed and the results compared to physician assessments of the PET/CT images.
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| ID | Title | Description |
|---|---|---|
| BG000 | Dynamic Arm | Participants that were already scheduled for a standard of care PET/CT study at a single institution could be included in this study. Those that chose to consent for this study had device sensors placed on the skin in four separate locations. The sensors could detect radiotracer near the injection site that was unavailable for circulation. During the 60 minute uptake, these subjects were scanned. After the 60 minute uptake period, the sensors were removed and participants continued with the normal PET/CT procedure. Participants also completed a questionnaire about the detector comfort. Dynamic arm (n=24 where 21 were analyzed) had 3 subjects that could not be analyzed due to technical errors, so 21 subjects were analyzed from this arm. Age and gender were not considered confounding factors and were not collected as part of the clinical study. |
| Units | Counts |
|---|---|
| Participants |
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| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Customized | 18 to 90 years (adults only). Participant age was not collected as part of this clinical study as long as these participants were within the 18 to 90 year range. |
| 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 | Number of Participants With Intraveneous Infiltration of FDG During Routine PET/CT Imaging by Visually Assessment of Interpreting Physicians | Infiltrations of 18F-2-fluoro-2-deoxy-D-glucose fluorodeoxyglucose (FDG) during Positron Emission Tomography (PET) radiotracer administration can lead to sub-optimal images. We aim to compare rates of radiotracer presence near the injection site detected by physicians. Every subject that participates in an FDG-PET scan received an intervenous injection as part of this study. The number of participants by arm were provided in Static Imaging Participants and Dynamic Imaging Participants. | Posted | Count of Participants | Participants | The time frame would be from the time the sensors were placed to the time the sensors were removed; no more than 2 hours. |
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The time frame would be from the time the sensors were placed to the time it took the subjects to respond to questions; no more than 2 hours.
Adverse events were collected during study participation. Participants completed a short questionnaire after participation to rate the pain of the sensor pads, pain of sensor placement, pain of sensor wires, and pain of removal of pads from skin.
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Dynamic Arm | This arm includes the study participants that participated in dynamic image acquisition. Dynamic images include multiple static images over a specified amount of time per image. |
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Limitations: How the reading physicians visually assessed the radioactivity presence at the injection site may not consistently compare to the quantitative TACs. The motion of the patient during sensor measurement may affect measurements.
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Medhat Osman, MD, PhD - Professor of Radiology, Director of Nuclear Medicine and PET/CT | Saint Louis University | 314-577-8047 | medhat.osman@health.slu.edu |
| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| ICF | No | No | Yes | Informed Consent Form | Jan 30, 2017 | Nov 29, 2018 | ICF_000.pdf |
| Prot | Yes | No | No | Study Protocol | Feb 14, 2017 | Apr 25, 2019 | Prot_001.pdf |
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| ID | Term |
|---|---|
| D016503 | Drug Delivery Systems |
| ID | Term |
|---|---|
| D004358 | Drug Therapy |
| D013812 | Therapeutics |
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All participants are included in the static imaging arm. Some participants were also included in the dynamic imaging arm
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| Percentage of Participants With Infiltrations Identified by Physicians and Sensor Device | The percentage of participants with infiltrations identified by physicians compared with those identified by the Lucerno sensor device as a measure of agreement between the two methods. | The time frame would be from the time the sensors were placed to the time the sensors were removed; no more than 2 hours. |
| 30443549 | Derived | Lattanze RK, Osman MM, Ryan KA, Frye S, Townsend DW. Usefulness of Topically Applied Sensors to Assess the Quality of 18F-FDG Injections and Validation Against Dynamic Positron Emission Tomography (PET) Images. Front Med (Lausanne). 2018 Nov 1;5:303. doi: 10.3389/fmed.2018.00303. eCollection 2018. |
| Published article: The Importance of Quality Control for Clinical PET Imaging | View source |
| BG001 | Static Arm | Participants that were already scheduled for a standard of care PET/CT study at a single institution could be included in this study. Those that chose to consent for this study had device sensors placed on the skin in four separate locations. The sensors could detect radiotracer near the injection site that was unavailable for circulation. After the 60 minute uptake period, the sensors were removed and participants continued with the normal PET/CT procedure. Participants also completed a questionnaire about the detector comfort. The static arm included 109 subjects. Age and gender were not considered confounding factors and were not collected as part of the clinical study. |
| BG002 | Total | Total of all reporting groups |
Participant age was not included in analysis. The inclusion/exclusion criteria included that the subjects must be greater than or equal to 18 years and less than or equal to 90 years. Once the age was verified during the consent process, the specific age of the subject was not included in analysis. |
| Count of Participants |
| Participants |
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| Sex/Gender, Customized | The genders included in this study were male and female. Participant gender was not collected as part of this clinical study. | Participant gender was not included in analysis. Al genders were included in the inclusion/exclusion criteria, so this data was not recorded nor included in analysis. | Count of Participants | Participants |
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| Race and Ethnicity Not Collected | Race and Ethnicity were not collected from any participant. | Count of Participants | Participants |
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| Region of Enrollment | Count of Participants | Participants |
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| Scheduled for a standard of care PET/CT | Count of Participants | Participants |
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| OG001 | Static Arm | This arm includes the study participants that participated in static image acquisition. |
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| Secondary | Number of Participants With Lucerno Sensor Device Detected Presence and/or Absence of Intravenous Infiltration | Review collected Lucerno sensor graphical data. The Lucerno time activity curves will capture an amount of activity from the sensors and assess subjects for presence or absence of infiltration at injection site. | The Time Activity Curve was studied that was provided from the sensor device among patients who underwent dynamic and static imaging. | Posted | Count of Participants | Participants | The time frame would be from the time the sensors were placed to the time the sensors were removed; no more than 2 hours. |
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| Secondary | Percentage of Participants With Infiltrations Identified by Physicians and Sensor Device | The percentage of participants with infiltrations identified by physicians compared with those identified by the Lucerno sensor device as a measure of agreement between the two methods. | Posted | Number | percentage of participants | The time frame would be from the time the sensors were placed to the time the sensors were removed; no more than 2 hours. |
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| 0 |
| 24 |
| 0 |
| 24 |
| 0 |
| 24 |
| EG001 | Static Arm | This arm includes the study participants that participated in static image acquisition. | 0 | 109 | 0 | 109 | 0 | 109 |
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