Evaluation of Gixam's Performance in a FIT Negative Population

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age45-85
SponsorJubaan Ltd.

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Subjects aged 45-85 years.

Able to provide a signed informed consent.

Scheduled for a screening colonoscopy at the investigation site.

Disqualifiers

Undergoing diagnostic colonoscopy for investigation of symptoms.

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.

History of colorectal cancer.

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

Trial design

Design model

Single group

Treatments tested in this trial

  • colorectal cancer (CRC) screening

    Device

    Gixam test

  • colorectal cancer screening

    Diagnostic test

    Fecal Immunochemistry Test (FIT)

  • Colonoscopy after bowel cleansing

    Procedure/Surgery

    Standard of care optical colonoscopy for colorectal cancer screening

Treatment groups

400 Participants
are divided into 1 treatment group
Group A: Single armExperimental treatment 3 interventions

Trial outcomes

Primary outcomes

1

Safety - number of device related adverse events and serious adverse events

Number of device related adverse events and serious adverse events

Time frame
Through study completion, up to 30 days
2

Efficacy - Gixam's sensitivity and specificity

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.

Time frame
Through study completion, up to 30 days

Secondary outcomes

Other outcomes

Sponsors and contacts

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