A single-center prospective observational study evaluates the correlation between an AI-based bowel preparation quality score (FQ-BBPS\[25%\]), which quantifies fecal coverage area during colonoscopy withdrawal, and the adenoma detection rate (ADR) in screening/surveillance patients.
Eligibility
Sex
ALL
Min age
45 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria:
* aged 45-75 years
* No colonoscopy within the past 3 years
Exclusion Criteria:
* Patients scheduled for therapeutic colonoscopy, postoperative surveillance after colorectal surgery, or treatment of histologically confirmed polyps
* Patients with highly suspected or pathologically confirmed colorectal cancer
* Patients presenting with alarm symptoms or signs (hematochezia, melena, unexplained anemia or weight loss, palpable abdominal mass, or a positive digital rectal examination)
* Pregnant or breastfeeding women
* Patients with gastrointestinal obstruction
* Patients with inflammatory bowel disease, familial adenomatous polyposis, or serrated polyposis syndrome
* Patients who have taken anticoagulants (e.g., aspirin, warfarin) within 7 days before colonoscopy or who have coagulation disorders
* Failed cecal intubation due to any cause other than excessive feces preventing intubation (e.g., obstructive lesions preventing scope passage, or patient intolerance to the procedure).
* Use of non-guideline-recommended bowel preparation agents
* Patients undergoing emergency colonoscopy
Primary outcome measure(s)
adenoma detection rate — 2 weeks after the procedure
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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