Efficacy of Gamma Camera Used Intraoperatively for ID of Sentinel Lymph Nodes w/ Lymphoscintigraphy
Primary Purpose
Multiple Myeloma, Breast Cancer
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Prototype intraoperative handheld gamma camera (pIHGC)
Lymphoscintigraphy with intraoperative gamma probes (GP)
radioactive Tc99M
Sponsored by
About this trial
This is an interventional diagnostic trial for Multiple Myeloma
Eligibility Criteria
INCLUSION CRITERIA
- Malignancy for which sentinel node biopsy with lymphoscintigraphy are indicated as part of the standard of care for tumor staging
- Age 18 or greater.
- Healthy enough for surgery
- Able to understand and willing to sign a written informed consent document.
EXCLUSION CRITERIA
- No exclusion requirements due to co-morbid disease or intercurrent illness.
- Documented allergy to colloid.
- Lymphoscintigraphy presents excessive high risk, eg, a consideration if pregnant or lactating
Sites / Locations
- Stanford University School of Medicine
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Intraoperative handheld Gamma Camera (pIHGC)
Gamma probes (GP)
Arm Description
The prototype intraoperative handheld gamma camera (pIHGC)
Standard of care intraoperative gamma probes (GP) currently in use.
Outcomes
Primary Outcome Measures
Relative Node Detection Sensitivity
Relative node detection sensitivity (S) was defined as the proportion of sentinel lymph nodes (SLNs) that were identified with each instrument, with the proportion determined as the number of true positives (TP) divided by the total evaluated (N). The outcome result is expressed as the percentage for each device with 95% confidence intervals.
Secondary Outcome Measures
Full Information
NCT ID
NCT01314963
First Posted
March 11, 2011
Last Updated
March 29, 2018
Sponsor
Stanford University
Collaborators
Whitaker Foundation
1. Study Identification
Unique Protocol Identification Number
NCT01314963
Brief Title
Efficacy of Gamma Camera Used Intraoperatively for ID of Sentinel Lymph Nodes w/ Lymphoscintigraphy
Official Title
Efficacy of a Novel, High-Sensitivity, Portable, Hand-Held Gamma Camera Used Intraoperatively for Identification of Sentinel Lymph Nodes With Lymphoscintigraphy
Study Type
Interventional
2. Study Status
Record Verification Date
March 2018
Overall Recruitment Status
Completed
Study Start Date
June 2008 (Actual)
Primary Completion Date
July 26, 2012 (Actual)
Study Completion Date
July 26, 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Stanford University
Collaborators
Whitaker Foundation
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study evaluates the ability of a prototype intraoperative handheld gamma camera (pIHGC) to image (detect) sentinel lymph nodes (SLNs) in melanoma and breast cancer during surgical excision, as compared to standard of care intraoperative gamma probes (GP). The unit of study in this trial was SNLs rather individual participants. Each device was assessed for relative node detection sensitivity (S) of those SLNs.
Detailed Description
Lymphoscintigraphy is an accepted and commonly-performed procedure used for staging of certain cancers, especially melanoma and breast cancer. It involves injecting a small amount of radioactivity under the skin in order to identify lymph nodes which should be biopsied (ie, the "sentinel lymph node, SLN") to determine if cancer has spread. The study objective was to evaluate the potential benefit of a new, camera-based technology (prototype device) which allows actual images to be obtained intra-operatively in the identification of sentinel nodes.
Each device was assessed for relative node detection sensitivity (S), defined as the proportion of sentinel lymph nodes (SLNs) that were identified with each instrument, with the proportion determined as the number of true positives (TP) divided by the total evaluated (N).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Myeloma, Breast Cancer
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
The unit of study in this trial was sentinel lymph nodes (SLNs) rather individual participants. with the comparison conducted by evaluation of each SLN with the prototype intraoperative handheld gamma camera (pIHGC) and standard of care intraoperative gamma probes (GP).
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
50 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Intraoperative handheld Gamma Camera (pIHGC)
Arm Type
Experimental
Arm Description
The prototype intraoperative handheld gamma camera (pIHGC)
Arm Title
Gamma probes (GP)
Arm Type
Active Comparator
Arm Description
Standard of care intraoperative gamma probes (GP) currently in use.
Intervention Type
Device
Intervention Name(s)
Prototype intraoperative handheld gamma camera (pIHGC)
Intervention Description
The prototype intraoperative handheld gamma camera (pIHGC) consists of a parallel-hole lead collimator coupled to a pixilated sodium iodide-thallium [NaI(Tl)] scintillation crystal array, itself coupled to a flat panel, multi-anode Hamamatsu H8500 position-sensitive photomultiplier tube. The collimator is 5x5 cm2 large in area and 1.5 cm thick, with 1.3 mm hexagonal holes and 0.2 mm septa. The 1.7 mm pitch crystal array is composed of 29x29 individual crystals, each 1.5x1.5x6 mm3 in size.
Intervention Type
Device
Intervention Name(s)
Lymphoscintigraphy with intraoperative gamma probes (GP)
Intervention Description
Lymphoscintigraphy with standard of care intraoperative gamma probes (GP)
Intervention Type
Radiation
Intervention Name(s)
radioactive Tc99M
Intervention Description
Lymphoscintigraphy involves injection of 0.4 to 1.0 mCi of radioactive Tc99M sulfur colloid around at the tumor site.
Primary Outcome Measure Information:
Title
Relative Node Detection Sensitivity
Description
Relative node detection sensitivity (S) was defined as the proportion of sentinel lymph nodes (SLNs) that were identified with each instrument, with the proportion determined as the number of true positives (TP) divided by the total evaluated (N). The outcome result is expressed as the percentage for each device with 95% confidence intervals.
Time Frame
1 day
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
INCLUSION CRITERIA
Malignancy for which sentinel node biopsy with lymphoscintigraphy are indicated as part of the standard of care for tumor staging
Age 18 or greater.
Healthy enough for surgery
Able to understand and willing to sign a written informed consent document.
EXCLUSION CRITERIA
No exclusion requirements due to co-morbid disease or intercurrent illness.
Documented allergy to colloid.
Lymphoscintigraphy presents excessive high risk, eg, a consideration if pregnant or lactating
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
John B Sunwoo, MD
Organizational Affiliation
Stanford University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Stanford University School of Medicine
City
Stanford
State/Province
California
ZIP/Postal Code
94305
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
24239343
Citation
Olcott P, Pratx G, Johnson D, Mittra E, Niederkohr R, Levin CS. Clinical evaluation of a novel intraoperative handheld gamma camera for sentinel lymph node biopsy. Phys Med. 2014 May;30(3):340-5. doi: 10.1016/j.ejmp.2013.10.005. Epub 2013 Nov 14.
Results Reference
result
Learn more about this trial
Efficacy of Gamma Camera Used Intraoperatively for ID of Sentinel Lymph Nodes w/ Lymphoscintigraphy
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