Completed NCT05414448

Combination of Artificial Intelligence and Mucosal Exposure Device to Enhance Colorectal Neoplasia Detection

Colorectal CancerN/AStage IIIStage IV

The investigators hypothesize that the combined use of CADe system (ENDOAID) and mucosal exposure device (Endocuff Vision®) would improve the adenoma detection rate when compared to CADe system alone.

Conditions: Adenoma, Colorectal Cancer, Colorectal Neoplasms

Eligibility Criteria

Inclusion Criteria

  • Aged 45-85 years old;
  • They require elective colonoscopy for colorectal cancer screening, polyp surveillance, or investigation of symptoms such as anemia or altered bowel habit;
  • Written informed consent obtained.

Exclusion Criteria

  • Contraindication to colonoscopy (e.g. intestinal obstruction or perforation)
  • Contraindication or conditions precluding polyp resection (e.g. active gastrointestinal bleeding, uninterrupted anticoagulation or dual antiplatelets)
  • Staged procedure for polypectomy or biopsy of known unresected lesions
  • Previous surgical resection of colon
  • Personal history of colorectal cancer
  • Personal history of familial polyposis syndrome
  • Personal history of inflammatory bowel disease
  • Advanced comorbid conditions (defined as American Society of Anesthesiologists grade 4 or above)
  • Pregnancy
  • Unable to obtain informed consent

Eligibility criteria are kept as the original English records from ClinicalTrials.gov; actual eligibility is determined by the research team's formal assessment and the informed consent form. Source: ClinicalTrials.gov, updated automatically every two weeks. Last synced: 2026年10月8日.