Video/Image Library of Endoscopy Procedures for the Development of AI-empowered Endoscopy Quality… (NCT06822816) | Clinical Trial Compass
RecruitingNot Applicable
Video/Image Library of Endoscopy Procedures for the Development of AI-empowered Endoscopy Quality Reporting and Educational Modules
Canada10,000 participantsStarted 2022-06-10
Plain-language summary
The goal of this observational study is to establish a video/image library dataset of complete endoscopy or partial colonoscopy procedures for patients with rectal cancer or inflammatory bowel disease (IBD). With this video/image library, the aims are:
* to develop and validate novel AI-empowered solutions to automatically detect and report endoscopy quality metrics
* to develop automated endoscopy reporting solutions, auditing, and educational tools for residents and fellows to enhance their endoscopy skills.
The hypothesis is that a heterogeneous video/image library will provide:
* comprehensive and robust source material to develop AI models
* real-time quality feedback at the end of an endoscopy procedure.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* ≥ 18 y.o.
* indication of undergoing a screening, surveillance, diagnostic, or therapeutic upper (EGD) or lower (colonoscopy) endoscopy
Exclusion Criteria:
* Coagulopathy defined as an elevated INR ≥ 2.5
* Platelet count ≤ 50,000/mm3
* Emergency endoscopy
* Poor general health defined as the American Society of Anesthesiologists physical status class \>3
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
EGD documented data
Timeframe: From enrollment to 14 days post-procedure
2
Colonoscopy documented data
Timeframe: From enrollment to 14 days post-procedure
Trial details
NCT IDNCT06822816
SponsorCentre hospitalier de l'Université de Montréal (CHUM)