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NCT05414448Completed

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

Combination of Artificial Intelligence (ENDOAID) and Mucosal Exposure Device (ENDOCUFF) to Enhance Colorectal Neoplasia Detection: a Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 22 Apr 2026

Brief summary (registry, in English)

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.

Status (registry)
Completed
Study type
Interventional
Enrollment
1726 (actual)
First submitted
8 Jun 2022
Start date
7 Mar 2023
Primary completion date
7 Jul 2025
Lead sponsor
Chinese University of Hong Kong
NCT number
NCT05414448

What you commit to

  • Study type: Interventional
  • Participants enrolled: 1726
  • From 7 Mar 2023 to the primary completion date, 7 Jul 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous surgical resection of colon

Other illness

  • 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)
  • 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)

Other

  • Staged procedure for polypectomy or biopsy of known unresected lesions
  • Pregnancy
  • Unable to obtain informed consent

Who the study is looking for

  • 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.

Age in the registry: 45 years to 85 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Prince of Wales Hospital
Coordinator of this site? Confirm its status
ShatinHong Kong SAR ChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.