Volumetric Laser Endomicroscopy With Intelligent Real-time Image Segmentation (IRIS)
Primary Purpose
Barrett's Esophagus Without Dysplasia, Barrett's Esophagus With Dysplasia, Barrett's Esophagus With Low Grade Dysplasia
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
IRIS (Intelligent real-time image segmentation)
VLE (Volumetric laser endomicroscopy)
Sponsored by
About this trial
This is an interventional diagnostic trial for Barrett's Esophagus Without Dysplasia focused on measuring VLE, Volumetric laser endomicroscopy, IRIS, Intelligent real-time image segmentation, Barrett's Esophagus
Eligibility Criteria
Inclusion Criteria:
- 18 years of age or older at the time of informed consent
- Barrett's esophagus greater than 2 cm in length
- Undergoing a scheduled upper endoscopy with VLE exam for surveillance as standard of care
Exclusion Criteria:
- Less than 18 years old at the time of informed consent
- Unable to provide written informed consent
- Esophageal stenosis/stricture preventing VLE
- Esophagitis
- Severe medical comorbidities preventing endoscopy
- Pregnancy
- Uncontrolled coagulopathy
Sites / Locations
- Mayo Clinic
- Mayo Clinic
- North Shore University Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
VLE without IRIS, followed by VLE with IRIS
VLE with IRIS, followed by VLE without IRIS
Arm Description
VLE (Volumetric laser endomicroscopy) performed alone, followed by IRIS (Intelligent real-time image segmentation) imaging.
VLE (Volumetric laser endomicroscopy) performed with IRIS (Intelligent real-time image segmentation) imaging, followed by VLE alone.
Outcomes
Primary Outcome Measures
Time for Image Interpretation (Mean)
The length of time required to fully assess and interpret the results of a VLE scan. Time will be a surrogate for ease of interpretation. Time will be recorded from start of image interpretation to the end of image interpretation. Length of the Barrett's segment will be taken into account (time per cm of Barrett's) when comparing this outcome between patients and procedures.
Time for Image Interpretation (Mean - Scaled)
The length of time required to fully assess and interpret the results of a VLE scan. Time will be a surrogate for ease of interpretation. Time will be recorded from start of image interpretation to the end of image interpretation. Length of the Barrett's segment will be taken into account (time per cm of Barrett's) when comparing this outcome between patients and procedures.
Time for Image Interpretation (Median - Scaled)
The length of time required to fully assess and interpret the results of a VLE scan. Time will be a surrogate for ease of interpretation. Time will be recorded from start of image interpretation to the end of image interpretation. Length of Barrett's will be taken into account (time per cm of Barrett's) when comparing this outcome between patients and procedures.
Secondary Outcome Measures
Subjects With Dysplasia on Biopsies
Biopsy yield (in terms of dysplasia present versus not present) of subjects with IRIS biopsies (double laser mark) will be compared to subjects with VLE without IRIS biopsies (single laser mark) and subjects with random biopsies (taken every 1cm in a four quadrant fashion throughout the length of the Barrett's).
Full Information
NCT ID
NCT03814824
First Posted
January 8, 2019
Last Updated
September 12, 2022
Sponsor
Northwell Health
Collaborators
NinePoint Medical, Mayo Clinic
1. Study Identification
Unique Protocol Identification Number
NCT03814824
Brief Title
Volumetric Laser Endomicroscopy With Intelligent Real-time Image Segmentation (IRIS)
Official Title
Volumetric Laser Endomicroscopy With Intelligent Real-time Image Segmentation (IRIS): a Multi-center Randomized Prospective Study
Study Type
Interventional
2. Study Status
Record Verification Date
September 2022
Overall Recruitment Status
Completed
Study Start Date
January 23, 2019 (Actual)
Primary Completion Date
May 31, 2020 (Actual)
Study Completion Date
February 28, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Northwell Health
Collaborators
NinePoint Medical, Mayo Clinic
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
No
5. Study Description
Brief Summary
This is a prospective randomized clinical trial examining how IRIS (Intelligent Real-time Image Segmentation) affects biopsy patterns in VLE (Volumetric laser endomicroscopy).
Detailed Description
Patients will undergo a VLE exam with and without IRIS per the standard of care. All patients regardless of the study participation in this study would receive VLE with and without IRIS clinically. They will be randomized into VLE without IRIS first vs VLE with IRIS first. The BUDDY Randomization System, provided for use by the Northwell Health Biostatistics Unit, will be used for this. Randomization will be stratified based on prior diagnosis of dysplasia. The order in which the patient is randomized to will be recorded on the case report form. There will be concealed allocation as the study coordinator performing the randomization will not know the order of the next allocation.
Both VLE and IRIS imaging are being performed as standard of care. However, randomization of the order allows for comparison of the two. Regions of interest (ROI) will be recorded using a full scan and recorded on the case report form. The time to identification of ROIs will also be recorded. Each group will then cross over such that the VLE without IRIS group will then have IRIS turned on. ROI will then be recorded for each group based on full scans. A consensus ROI will be recorded based on the two exams. Only one ROI per centimeter will be allowed to avoid overlapping of laser marks. In addition, VLE without IRIS and IRIS marks within 75 frames of each other or 2 hours (on a clock face orientation) will be considered the same target.
Laser marking will then be performed. A double laser mark will be applied to all IRIS ROIs. A single laser mark will be applied to VLE ROIs. Targeted biopsies will be taken of all laser marks and placed in separate biopsy jars. Biopsies will be taken in between the laser marks for double laser marked areas. For single laser marks, biopsies will be taken on either side of the laser mark. Resection of visible lesions will then occur per standard of care (if present) followed by random biopsies of the segment. Random biopsies are pinch biopsies every 1 cm the length of the Barrett's in a 4 quadrant fashion per gastrointestinal society guidelines. There are no additional research biopsies being performed outside this study. The targeted biopsies are based on the VLE features that are suspicious for dysplasia and thus standard of care. The other biopsies being performed here are random biopsies which are also being performed for standard of care. Biopsied samples will be stored per standard of care procedures per the pathology department. They will not be stored for future research purposes.
Following each procedure, the physician will be asked a series of Likert Scale questions to assess the utility of IRIS in that procedure, including how it impacts their confidence in image interpretation, their ability to assimilate data more easily and quickly, and their overall perception of the technology.
Although, the VLE with IRIS and VLE without IRIS are being performed as standard of care, all adverse events will be recorded and reported to the IRB.
All data will be entered into a central encrypted REDCap database.
Expert pathologists who specialize in gastrointestinal pathology will read the histology. A second gastrointestinal pathologist will confirm any histologic diagnosis of dysplasia. This is the standard of care at Northwell Health and academic medical centers per gastrointestinal society guidelines.
All procedures (upper endoscopy, volumetric laser endomicroscopy, and IRIS enhanced VLE) will be performed as standard of care. The prospective data collection and initial randomization will be the research component. All data collected will be de-identified before being transferred into a database. This will be kept in a safe place that is only accessible to the research team.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Barrett's Esophagus Without Dysplasia, Barrett's Esophagus With Dysplasia, Barrett's Esophagus With Low Grade Dysplasia, Barrett's Esophagus With High Grade Dysplasia, Barrett's Esophagus With Dysplasia, Unspecified
Keywords
VLE, Volumetric laser endomicroscopy, IRIS, Intelligent real-time image segmentation, Barrett's Esophagus
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
148 (Actual)
8. Arms, Groups, and Interventions
Arm Title
VLE without IRIS, followed by VLE with IRIS
Arm Type
Active Comparator
Arm Description
VLE (Volumetric laser endomicroscopy) performed alone, followed by IRIS (Intelligent real-time image segmentation) imaging.
Arm Title
VLE with IRIS, followed by VLE without IRIS
Arm Type
Active Comparator
Arm Description
VLE (Volumetric laser endomicroscopy) performed with IRIS (Intelligent real-time image segmentation) imaging, followed by VLE alone.
Intervention Type
Diagnostic Test
Intervention Name(s)
IRIS (Intelligent real-time image segmentation)
Intervention Description
IRIS has the ability to identify and display three specific images features that may correlate with dysplasia that are represented in different color schemes.
Intervention Type
Diagnostic Test
Intervention Name(s)
VLE (Volumetric laser endomicroscopy)
Intervention Description
VLE uses infrared light to produce real time high-resolution cross sectional imaging of the esophagus.
Primary Outcome Measure Information:
Title
Time for Image Interpretation (Mean)
Description
The length of time required to fully assess and interpret the results of a VLE scan. Time will be a surrogate for ease of interpretation. Time will be recorded from start of image interpretation to the end of image interpretation. Length of the Barrett's segment will be taken into account (time per cm of Barrett's) when comparing this outcome between patients and procedures.
Time Frame
Index procedure, up to 1 hour
Title
Time for Image Interpretation (Mean - Scaled)
Description
The length of time required to fully assess and interpret the results of a VLE scan. Time will be a surrogate for ease of interpretation. Time will be recorded from start of image interpretation to the end of image interpretation. Length of the Barrett's segment will be taken into account (time per cm of Barrett's) when comparing this outcome between patients and procedures.
Time Frame
Index procedure, up to 1 hour
Title
Time for Image Interpretation (Median - Scaled)
Description
The length of time required to fully assess and interpret the results of a VLE scan. Time will be a surrogate for ease of interpretation. Time will be recorded from start of image interpretation to the end of image interpretation. Length of Barrett's will be taken into account (time per cm of Barrett's) when comparing this outcome between patients and procedures.
Time Frame
Index procedure, up to 1 hour
Secondary Outcome Measure Information:
Title
Subjects With Dysplasia on Biopsies
Description
Biopsy yield (in terms of dysplasia present versus not present) of subjects with IRIS biopsies (double laser mark) will be compared to subjects with VLE without IRIS biopsies (single laser mark) and subjects with random biopsies (taken every 1cm in a four quadrant fashion throughout the length of the Barrett's).
Time Frame
Index procedure
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
18 years of age or older at the time of informed consent
Barrett's esophagus greater than 2 cm in length
Undergoing a scheduled upper endoscopy with VLE exam for surveillance as standard of care
Exclusion Criteria:
Less than 18 years old at the time of informed consent
Unable to provide written informed consent
Esophageal stenosis/stricture preventing VLE
Esophagitis
Severe medical comorbidities preventing endoscopy
Pregnancy
Uncontrolled coagulopathy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Arvind Trindade, MD
Organizational Affiliation
Northwell Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mayo Clinic
City
Scottsdale
State/Province
Arizona
ZIP/Postal Code
85259
Country
United States
Facility Name
Mayo Clinic
City
Rochester
State/Province
Minnesota
ZIP/Postal Code
55905
Country
United States
Facility Name
North Shore University Hospital
City
Manhasset
State/Province
New York
ZIP/Postal Code
11030
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
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Volumetric Laser Endomicroscopy With Intelligent Real-time Image Segmentation (IRIS)
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