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Comparison of adenoma detection rates with 6 minutes of AI-assisted withdrawal and 9 minutes of standard withdrawal: a multicenter randomized controlled non-inferiority study

Comparison of adenoma detection rates with 6 minutes of AI-assisted withdrawal and 9 minutes of standard withdrawal: a multicenter randomized controlled non-inferiority study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600119423
Enrollment
Unknown
Registered
2026-02-26
Start date
2026-03-01
Completion date
Unknown
Last updated
2026-03-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal adenoma

Interventions

AI-assisted retraction 6 minutes group:After randomization, AI-assisted withdrawal was carried out, and the withdrawal time was controlled at 6 minutes
Standard 9-minute withdrawal group:After random enrollment, a routine withdrawal operation without artificial intelligence assistance was performed, and the withdrawal time was controlled within 9 min

Sponsors

The Tenth People's Hospital Affiliated to Tongji University (Shanghai Tenth People's Hospital)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1) Male or female, age 40-75 years old 2) Patients with colorectal endoscopy (including screening, monitoring and diagnosis). 3) Good self-evaluation of bowel preparation (watery or watery stools without residue) 4) Agree to participate in this clinical trial and sign the informed consent form

Exclusion criteria

Exclusion criteria: 1) Patients with clinically suspected or confirmed colorectal cancer (abdominal mass, positive digital rectal examination, weight loss or anemia without apparent cause). 2) Patients with abnormal coagulation function, or who are taking antiplatelet drugs or anticoagulant drugs in the past 7 days 3) inflammatory bowel disease or polyp syndrome 4) History of colectomy or abdominal surgery 5) Those with severe diseases or other high-risk conditions who cannot tolerate endoscopy 6) Any other factors that are not suitable for inclusion or affect the subject's participation in the study

Design outcomes

Primary

MeasureTime frame
adenoma detection rate;

Secondary

MeasureTime frame
Polyp detection rate;Number of polyps detected in a single colonoscopy;Detection rate of advanced adenoma;Detection rate of sessile serrated lesions;

Countries

China

Contacts

Public ContactLiu Feng

The Tenth People's Hospital Affiliated to Tongji University (Shanghai Tenth People's Hospital)

drliuffeng@hotmail.com+86 136 8197 3214

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026