Evaluation of Gixam's Performance in a FIT Negative Population

Phase 2

Recruiting

• Conditions: Colorectal Adenoma; Colorectal Cancer (CRC); Colorectal Cancer (CRC) Screening
• Interventions: Device: colorectal cancer (CRC) screening; Diagnostic Test: colorectal cancer screening; Procedure: Colonoscopy after bowel cleansing

• Registration Number: NCT06612281
• Lead Sponsor: Jubaan Ltd.

Brief Summary

In the United States, colorectal cancer ranks second to lung cancer as a cause of cancer death and is the third most commonly occurring cancer in both men and women. Colorectal cancer in most cases develops slowly over a period of years, starting with the growth of precancerous polyps on the colon or rectum wall. The slow development of colorectal cancer makes it possible to detect and prevent it entirely by the removal of the precancerous polyps with colonoscopy. To date, there is no screening test, other than colonoscopy, able to detect the precancerous polyps. Gixam is a camera that takes multiple pictures of your tongue and uses artificial intelligence software to predict the presence of precancerous polyps within your colon or rectum that may eventually become cancerous.

The device creates the prediction by comparing the images taken of your tongue with many other images of tongues from healthy patients and patients with a history of precancerous polyps. Patients who have been predicted by Gixam to have precancerous polyps may be more likely to complete colonoscopy at the interval recommended by their physician, potentially reducing the likelihood of developing colorectal cancer.

The purpose of this research study is to test the accuracy of the Gixam device in persons that have received a negative outcome on a Fecal Immunochemical Test (FIT). This study will compare this prediction to the actual findings of your scheduled standard care colonoscopy and allow researchers to evaluate and improve the Gixam system.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2024-09-09
• Study First Submitted QC: 2024-09-22
• Study First Posted: 2024-09-25
• Status Verified: 2024-11
• Study Start: 2024-11-01
• Last Update Submitted: 2024-11-12
• Last Update Posted: 2024-11-14
• Primary Completion: 2025-03-30
• Study Completion: 2025-04-30

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 400

Inclusion Criteria

1. Subjects aged 45-85 years.
2. Able to provide a signed informed consent.
3. Scheduled for a screening colonoscopy at the investigation site.

Exclusion Criteria

1. Undergoing diagnostic colonoscopy for investigation of symptoms.

2. Has undergone colonoscopy within preceding nine (9) years except for a failed colonoscopy due to poor bowel preparation. Failed colonoscopy must have been within the past year and without therapeutic intervention.

3. History of colorectal cancer.

4. Family history of colorectal cancer, defined as having one or more first-degree relatives (parent, sibling, or child) with CRC at any age.

5. Subject has a diagnosis or medical / family history of any of the following conditions, including:

   • Familial adenomatous polyposis (also referred to as "FAP", including attenuated FAP and Gardner's syndrome),
   • Hereditary non-polyposis CRC syndrome (also referred to as "HNPCC" or "Lynch Syndrome"),
   • Other hereditary cancer syndromes including but are not limited to Peutz-Jeghers Syndrome, MYH-Associated Polyposis (MAP), Turcot's (or Crail's) Syndrome, Cowden's Syndrome, Juvenile Polyposis, Neurofibromatosis, or Familial Hyperplastic Polyposis.

6. Subject has a diagnosis or personal history of inflammatory bowel disease (IBD) including chronic ulcerative colitis and/or Crohn's disease.

7. Subjects with a disability to extend their tongue.

8. Subjects with tongue piercing.

9. Dental visit in the past 7 days prior to Gixam test.

10. Intake of pro-biotics over the past 3 months pre-Gixam test.

11. Subject has any condition that in the opinion of the Investigator should preclude participation in the study.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Single arm	colorectal cancer screening	All participants will undergo the same study procedures: FIT, Gixam, and colonoscopy
Single arm	Colonoscopy after bowel cleansing	All participants will undergo the same study procedures: FIT, Gixam, and colonoscopy
Single arm	colorectal cancer (CRC) screening	All participants will undergo the same study procedures: FIT, Gixam, and colonoscopy

Primary Outcome Measures

Name	Time	Method
Safety - number of device related adverse events and serious adverse events	Through study completion, up to 30 days	Number of device related adverse events and serious adverse events
Efficacy - Gixam's sensitivity and specificity	Through study completion, up to 30 days	Gixam's sensitivity and specificity to predict the presence of colorectal adenoma or sessile serrated lesions (advances and non-advanced) / CRC in a FIT negative population.

Trial Locations

Locations (1)

The Oregon Clinic Gastroenterology-East; 🇺🇸 Portland, Oregon, United States