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AzTrials

Colorectal CancerCOLODETECT2NCT05594576

Comparison of the ENDOCUFF VISION® Endoscopy Cap Coupled With GI GENIUS™ Artificial Intelligence Compared to Each Device Alone in Improving Colonic Adenoma Detection Rate During Colonoscopy

A study testing GI GENIUS™ artificial intelligence system and ENDOCUFF VISION® endoscopic cap in people with Colorectal Cancer and Adenoma, run by Centre Hospitalier Universitaire de Nīmes at 2 sites in France.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Colorectal cancer is the 2nd most common cause of death by cancer. Screening is therefore essential, with a positive impact for prevention, and in the visualization and removal of colonic adenomas, pre-cancerous lesions of colorectal cancer. Read more about this study

Who is it for?
Ages 18 to 85 years
Conditions the study is for
Colorectal Cancer, Adenoma, Intestinal Polyps
What is being tested?
GI GENIUS™ artificial intelligence system and ENDOCUFF VISION® endoscopic cap
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
481 participants
Where
2 sitesFrance
Study dates
18 Oct 2022to 11 Oct 2024
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 85 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Need to perform colorectal cancer screening colonoscopy:
  • Primary Screening: Fecal Immunological Test positive;
  • Secondary screening: personal or family history of polyps, personal or family history of colorectal cancer, rectorrhagia-like symptomatology.
  • Patient candidate for outpatient management.
  • Patient who has given free and informed consent.
  • Patient who has signed the consent form.
  • Patient affiliated or beneficiary of a health insurance plan.

Who cannot join

  • The subject is participating in a category 1 interventional study, or is in a period of exclusion determined by a previous study
  • The subject refuses to sign the consent
  • It is impossible to give the subject informed information
  • The patient is under safeguard of justice or state guardianship
  • History of inflammatory bowel disease, Crohn's disease.
  • Failure of a previous colonoscopy.
  • Known familial polyposis.
  • Contraindication to polypectomy (coagulation disorder, treatment with CLOPIDOGREL / anticoagulant).

Trial locations and contacts

2 sites in 1 country.

France2 sites
  • CHU de Limoges

    Limoges, 87000

  • CHU de Nîmes

    Nîmes

Other trials in France

About this study

Colorectal cancer is the 2nd most common cause of death by cancer. Screening is therefore essential, with a positive impact for prevention, and in the visualization and removal of colonic adenomas, pre-cancerous lesions of colorectal cancer.

The colonic adenoma detection rate (CADR), the gold standard for colonoscopy screening and screening studies, is the ratio of the number of colonoscopies with at least one histologically verified colonic adenoma to the total number of colonoscopies performed in a center. It varies between 25 and 45% depending on the center. There is a large inter-operator CADR variability, which has been linked to an increased incidence and excess mortality in colorectal cancers.

Read more

To improve this detection rate, several innovative techniques have been developed:

The endoscopic cap helps improve this detection rate: it is a 2cm tip with double row of plastic wings, fixed to the distal end of the colonoscope, which acts by unfolding the colonic haustrations allowing a better visualization of adenomas, and more particularly those of sessile morphology and sigmoidal location. Several multicenter studies have shown an improvement in the adenoma detection rate with this device compared to screening colonoscopy alone, with an adenoma detection rate optimization of 14%. Since then other devices, such as the Endocuff, have emerged with comparable efficacy. The Medtronic© GI GENIUS system integrates artificial intelligence (AI) to assist in the detection of polyps. It automatically identifies these precancerous lesions in real time.

The study investigators previously performed a retrospective pilot study (COLODETECT), comparing colonoscopy alone as a control group, against AI alone and against the combined cap + AI. This study showed encouraging results in terms of colonic adenoma detection rate (60% for the AI + cap group versus 37% for the AI alone group versus 33% for the colonoscopy alone group, p=0.037) However, it requires a higher level of evidence to be validated in practice. This prospective COLODETECT2 study estimated an a priori expected difference between A.I. - Cap and A.I. alone of about 15% CADR.

The GI GENIUS artificial intelligence system and the ENDOCUFF VISION endoscopic cap have separately proven their effectiveness in terms of colonic adenoma detection compared to colonoscopy alone. However, some limitations remain: existence of false positives (mucosal folds, residues), some morphological types still difficult to recognize (scalloped adenomas), non visualized colonic lesions.

This study therefore focuses on the possible complementarity of these 2 medical devices, in order to maximize the detection rate of colonic adenomas, and thus overcome the limitations of these two techniques by optimizing the visualization of these precancerous lesions, and consequently increasing the impact of colorectal cancer screening.

The study authors hypothesize that the combination of GI GENIUS™ AI coupled with the ENDOCUFF VISION® endoscopy cap provides a better colonic adenoma detection rate (CAD) during colonoscopy than either GI GENIUS™ AI alone or the ENDOCUFF VISION® cap alone.

Being tested
GI GENIUS™ artificial intelligence system, ENDOCUFF VISION® endoscopic cap
Keywords
colonoscopy
Medical subject headings
Colorectal Neoplasms, Adenoma, Intestinal Polyps

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • GI GENIUS™ artificial intelligence systemProcedure or surgery

    Device used during coloscopy for detection of colonic adenoma

  • ENDOCUFF VISION® endoscopic capProcedure or surgery

    Device used during coloscopy for detection of colonic adenoma

Study groups in NCT05594576
Study groupRoleWhat they receive
ENDOCUFF VISION® Endoscopic Cap coupled with GI GENIUS™ Artificial Intelligence (AI)ExperimentalNot described
Receives: Procedure: GI GENIUS™ artificial intelligence system; Procedure: ENDOCUFF VISION® endoscopic cap
GI GENIUS™ Artificial Intelligence (AI) aloneActive comparatorNot described
ENDOCUFF VISION® endoscopic cap aloneActive comparatorNot described
Receives: Procedure: ENDOCUFF VISION® endoscopic cap

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Compare colonic adenoma detection rates (CADR) during colonoscopy between the three groups

    %; defined as the number of colonoscopies with detection of at least one colonic adenoma out of the total number of colonoscopies performed

    Measured: Day 0

Secondary outcomes (9)
  1. Operator effect on CADR, between the three groups, per operator

    CADR (%), defined as the number of colonoscopies with detection of at least one colonic adenoma out of the total number of colonoscopies performed for each strategy per operator

    Measured: Day 0

  2. CADR according to adenoma size, for each strategy

    CADR (%), detected by colonoscopy according to their size in mm (especially those smaller than 3 mm)

    Measured: Day 0

  3. CADR according to adenoma histology for each strategy.

    CADR (%), detected by colonoscopy according to histology (low/high grade dysplasia)

    Measured: Day 0

  4. CADR according to adenoma morphology for each strategy.

    CADR (%), detected by colonoscopy according to (Paris morphological classification: Ip, Is, IIa, IIb, IIc, III)

    Measured: Day 0

  5. Shrinkage time for the Genius groups.

    Measurement of withdrawal time (min, sec) for GI GENIUS™-Cap software or GI GENIUS™ software alone strategies (time from cecum to colonoscope removal).

    Measured: Day 0

  6. Rate of cecal intubation between groups

    % of exams in which the entire colon was examined.

    Measured: Day 0

  7. Progression time between groups

    Mean progression time (time from introduction of colonoscope to cecum; min, sec

    Measured: Day 0

  8. Operative time between groups

    Mean time from introduction of colonoscope to removal of endoscope from patient; min, sec

    Measured: Day 0

  9. The number of immediate intra- and postoperative adverse events (bleeding, perforation) according to the different strategies

    Collection of immediate intra- and postoperative adverse events (bleeding, perforation) for the three study strategies

    Measured: Day 0

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Oct 2022
  2. Study start18 Oct 2022
  3. Primary completion11 Oct 2024
  4. Study completion11 Oct 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Diagnosis
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
481 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05594576
Sponsor's protocol ID
NIMAO/2021-2/LC-01
Acronym
COLODETECT2
Status last verified
Dec 2025
First submitted
21 Oct 2022
Last updated
5 Dec 2025
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing GI GENIUS™ artificial intelligence system and ENDOCUFF VISION® endoscopic cap in people with Colorectal Cancer and Adenoma, run by Centre Hospitalier Universitaire de Nīmes at 2 sites in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 5 Dec 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Compare colonic adenoma detection rates (CADR) during colonoscopy between the three groups (time frame: Day 0). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 Dec 2025.

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