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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06305364
Other study ID # CL-1001
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date August 1, 2023
Est. completion date December 1, 2024

Study information

Verified date March 2024
Source Jubaan Ltd.
Contact Daniella Bleistein
Phone +9724643-2991
Email daniella@jubaan.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a prospective, multicenter, single-arm clinical investigation designed to evaluate the accuracy of the Gixam™ System in identifying subjects with colorectal adenomas compared to optical colonoscopy. Subjects arriving for a standard of care colonoscopy at the investigation site will be offered to participate in the study. Following an informed consent process, images of the subjects' tongue will be obtained with the Gixam™ System and a prediction score will be generated by the Gixam™ AI model. Subjects will thereafter proceed to their SOC colonoscopy, and the Gixam™ score will be compare with colonoscopy findings to evaluate its performance.


Recruitment information / eligibility

Status Recruiting
Enrollment 800
Est. completion date December 1, 2024
Est. primary completion date December 1, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: 1. Males or females 2. Age: 18-75 years, inclusive 3. Scheduled for colonoscopy procedure at investigation site subject to one of the below criteria: 1. Screening - defined as first colonoscopy or consecutive colonoscopy without previous findings, previous colonoscopy performed at least 10 years ago (- 1 year); 2. Patient with finding of colorectal adenoma or sessile serrated polyp in previous colonoscopy (must be documented in patient's medical history). 4. Able to comprehend and provide informed consent. Exclusion Criteria: 1. Subject who is not a suitable candidate for a colonoscopy 2. Lynch or Familial Adenomatous Polyposis (FAP) inherited syndromes 3. Current or previous Inflammatory Bowel Disease (IBD - Crohn's, Ulcerative Colitis) of significant duration 4. Patients with a disability to extend their tongue. 5. Patients with tongue piercings.

Study Design


Intervention

Device:
Gixam
Participants will be required to extend their tongue in the Gixam device. Six images will be obtained and analyzed by the artificial intelligence (AI) model generating a prediction score for the presence of colorectal adenoma.

Locations

Country Name City State
United States NewYork-Presbyterian / Columbia University Irving Medical Center New York New York
United States Westside GI New York New York

Sponsors (1)

Lead Sponsor Collaborator
Jubaan Ltd.

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Primary Safety Endpoint - Number of device related adverse events and serious adverse events 1 day
Primary Primary Efficacy Endpoint - Gixam's diagnostic accuracy Gixam's diagnostic accuracy (sensitivity and specificity) of adenomatous colorectal polyps.
The Gixam's predictive value will be compared to the patient's colonoscopy + pathology (if any specimens are collected) findings as ground truth on a binary basis (YES/NO for adenomatous and sessile serrated polyps).
14 days (till pathology report is received)
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