Actively Recruiting
COLO-PREDICT: Digital Training and Optical Diagnosis of Colorectal Polyps
Led by Clinique Paris-Bercy · Updated on 2026-02-23
1500
Participants Needed
1
Research Sites
29 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Colorectal cancer prevention relies on high-quality colonoscopy and accurate optical characterization of colorectal polyps. Optical diagnosis may allow optimization of management strategies such as resect-and-discard for diminutive polyps, potentially improving efficiency in routine practice. COLO-PREDICT is a prospective, single-center, observational study designed to evaluate the impact of a structured digital training program (Colo-ID, a digital application for colonic polyp characterisation training) on the accuracy of optical histology prediction of colorectal polyps in real-life clinical practice. All consecutive adult patients undergoing colonoscopy with at least one detected polyp will be included. Optical prediction of polyp histology will be recorded during the procedure. All polyps will be resected and sent for histopathological analysis according to standard practice. No modification of patient management will occur as part of the study. The primary objective is to assess the concordance between optical prediction and histopathology before and after implementation of the digital training program. Secondary objectives include evaluation of prediction performance according to polyp characteristics and assessment of potential implications for clinical practice.
CONDITIONS
Official Title
COLO-PREDICT: Digital Training and Optical Diagnosis of Colorectal Polyps
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 618 years
- Patients undergoing colonoscopy in routine clinical practice at the participating center
- At least one colorectal polyp detected during colonoscopy
- Optical histology prediction recorded during the procedure
- Histopathological analysis available for resected polyps (reference standard)
You will not qualify if you...
- Patients aged <18 years
- Refusal or opposition to use of data if applicable under local regulations
- Missing key study data such as no recorded optical prediction or no histopathology result
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Clinique Paris-Bercy
Charenton-le-Pont, Val de Marne, France, 94220
Actively Recruiting
Research Team
D
David Karsenti, MD
CONTACT
C
Coralie Declerck, Ms.
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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