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NCT07299071Recruiting

Efficacy of CAD in Screening Colonoscopy to Reduce the Risk of Advanced Adenoma at 3 Years.

Randomized Controlled Trial Evaluating the Efficacy of CAD in Screening Colonoscopy to Reduce the Risk of Advanced Adenoma at 3 Years.

Source: ClinicalTrials.gov · Last updated 24 Sept 2026

Brief summary (registry, in English)

The occurrence of interval cancers after colonoscopy raises the possibility of missed lesions. High- performance computer aided diagnosis (CAD) systems have been specially designed for the detection of colorectal lesions (CAD for detection is named CADe). The use of CADe improves adenoma detection in screening colonoscopy. The potential of CADe system in reducing the rate of progression to advanced polyps or interval cancer between two colonoscopies remains still uncertain.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
592 (estimated)
First submitted
9 Dec 2025
Start date
Mar 2026
Primary completion date
Mar 2031
Lead sponsor
University Hospital, Bordeaux
NCT number
NCT07299071

What you commit to

  • Study type: Interventional
  • Planned participants: 592
  • From Mar 2026 to the primary completion date, Mar 2031
  • 15 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • An infiltrative tumor was diagnosed during colonoscope insertion time, not accessible to endoscopic resection and likely to require surgical management (a procedure where part of the colon may need to be removed).

Other illness

  • Personal history of inflammatory bowel disease
  • Personal history of genetic predisposition of CRC
  • Personal history of major colorectal surgery involving total or subtotal colectomy

Other

  • Failed complete colonoscopy, defined by the absence of cecal intubation or identification of the terminal ileum.
  • Inadequate bowel preparation (Boston bowel preparation score \< 6, and/or least at one part of colon with score ≤ 1)
  • Patient under guardianship or protection
  • Pregnant women
  • Not fluent in French or illiterate

Who the study is looking for

  • Patients over 18 years of age with indication for colonoscopy as part of a screening program, after a positive immunological (FIT) test, and/or for personal or family history of colorectal cancer and/or personal history of colonic adenomas and/or sessile serrated polyp,
  • Written informed consent signed
  • Patients covered by a health-care insurance.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (15)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CH de la côte Basque
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BayonneFranceNot yet recruiting
CHU Brest la Cavale Blanche
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BrestFranceNot yet recruiting
Hôpital de Carhaix
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Carhaix-PlouguerFranceNot yet recruiting
Clinique Paris Bercy
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Charenton-le-PontFranceNot yet recruiting
CHU de Limoges
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LimogesFranceNot yet recruiting
Institut Paoli-Calmettes
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MarseilleFranceNot yet recruiting
Clinique Jules Verne
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NantesFranceNot yet recruiting
CHU Nîmes
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NîmesFranceNot yet recruiting
Aphp Hegp
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ParisFranceNot yet recruiting
APHP - Hôpital Saint Antoine
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ParisFranceNot yet recruiting
APHP - Hôpital Tenon
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ParisFranceNot yet recruiting
CHU Bordeaux - Hopital Haut-Leveque
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PessacFranceRecruiting
CHU de Rennes
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RennesFranceNot yet recruiting
Clinique Pasteur
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ToulouseFranceNot yet recruiting
CHRU de Nancy - Hôpital Brabois Adultes
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Vandœuvre-lès-NancyFranceNot yet recruiting

This page is information, not medical advice. Discuss any trial with your doctor.