Actively Recruiting
Colonoscopy TRaining With or Without Artificial INtelligence Among Endoscopy Residents
Led by University of Thessaly · Updated on 2026-02-19
10
Participants Needed
1
Research Sites
73 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Type of study: Randomized controlled study Investigated Procedure: Artificial Intelligence Software for Polyp Detection in Colonoscopy training Trial participants: Endoscopy trainees during their training with at least one year of training ahead and no previous structured exposure to CADe Objectives: Primary: Adenoma Miss Rate (AMR) in the end of the first year of training for each group and after the crossover. Secondary: Further endoscopists-related parameters will be recorded and compared between the two arms: PDR, ADR, aADR, PMR, withdrawal time, CIR, AEs The investigators will be asked, when possible, to follow-up the patients until they have their next colonoscopy or a diagnosis of CRC to assess for interval cancer.
CONDITIONS
Official Title
Colonoscopy TRaining With or Without Artificial INtelligence Among Endoscopy Residents
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Endoscopy trainees at any stage of training with at least one year of training remaining
- No previous structured exposure to computer-aided detection (CADe) during training
- Adult patients undergoing diagnostic, screening, or surveillance colonoscopy
- Signed and dated informed consent provided
- Age 18 years or older
- Ability to read and write in the provided language
- Able to comply with the trial protocol and provide written informed consent
You will not qualify if you...
- Endoscopy trainees after basic training, in their last year of training, or with systematic exposure to CADe
- Patients with known contraindications for biopsy, bowel obstruction, or perforation
- Pregnant or lactating females
- Patients with known polyposis syndromes, history of inflammatory bowel disease (IBD), colorectal cancer (CRC), or colorectal surgery
- Patients whose cecum is not reached and who are highly suspected of having polyposis syndromes, IBD, intestinal tuberculosis, or CRC
- Patients with incomplete bowel preparation (segmental Boston Bowel Preparation Score less than 2 or total score less than 6)
AI-Screening
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Trial Site Locations
Total: 1 location
1
General University Hospital of Larissa
Larissa, Greece
Actively Recruiting
Research Team
A
Apostolis Papaefthymiou
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
OTHER
Number of Arms
2
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