CAD EYE Detection of Remaining Lesions After EMR
Colorectal Dysplasia, Colorectal Neoplasms
About this trial
This is an interventional diagnostic trial for Colorectal Dysplasia focused on measuring Artificial Intelligence, Colonoscopy, Endoscopic mucosal resection, Computer-assisted diagnosis
Eligibility Criteria
Inclusion Criteria:
- Patients referred to our center with an indication of colonoscopy and EMR for the treatment of lesions suspicious of high-grade dysplasia and early invasive cancer.
- Patients who authorize EMR and colonoscopy.
- Signed informed consent
Exclusion Criteria:
- Any clinical condition which makes EMR inviable.
- Poor bowel preparation score defined as the total Boston bowel preparation score (BBPS) <6 and the right-segment score <2
- Patients with more than one previous EMR
- Lost on a three-month follow-up after EMR
- Pregnancy or nursing
Sites / Locations
- Carlos Robles-MedrandaRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Endoscopic mucosal resection + CAD-Eye™
Endoscopic mucosal resection without CAD Eye
This group constitutes patients with lesions suggestive of high-grade dysplasia or early invasive cancer approached with endoscopic mucosal resection, subjected to colonoscopy + CAD-Eye™ system evaluation for the detection of remaining malignant tissue. For this group, the investigators used as a complement tool an AI system (CAD-Eye™) for the detection of remaining lesions immediately after EMR and in a three-month follow-up.
This group constitutes patients with lesions suggestive of high-grade dysplasia or early invasive cancer approached with endoscopic mucosal resection and subjected to colonoscopy. The detection of remaining lesions immediately after EMR is based on the visual impression of the expert. For this group, the investigators used as a complement tool an AI system (CAD-Eye™) only for the evaluation of the post-procedure scar to detect remaining lesions in the three-month follow-up.