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Assessment of the effectiveness of a large language model focus on colonoscopy bowel preparation: a single-center, randomized controlled study

Assessment of the effectiveness of a large language model focus on colonoscopy bowel preparation: a single-center, randomized controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500102690
Enrollment
Unknown
Registered
2025-05-19
Start date
2025-05-25
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

bowel preparation of colonoscopy

Interventions

Group A: control group:Bowel preparation was performed according to the usual procedure, with the patient judging the bowel preparation as well as choosing whether or not to drink the remaining 1 lite
Group B: LLM-assisted bowel preparation group:After the patient transmits a photo of the feces to the LLM during bowel preparation, the bowel preparation is judged by the LLM as well as the choice of

Sponsors

Qilu Hospital of Shandong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients preparing for colonoscopy; 2. Male or female, aged 18-65 years.

Exclusion criteria

Exclusion criteria: 1. history of previous intestinal surgery; 2. gastroparesis or gastric outlet obstruction; 3. known or suspected intestinal obstruction or perforation; 4. severe chronic renal failure (creatinine clearance 180 mmHg and/or diastolic blood pressure >100 mmHg). 9. Moderate or massive active gastrointestinal bleeding (>100 ml/day); 10. major mental illness; 11. allergy to laxatives (e.g. polyethylene glycol); 12. Inability to give informed consent or unwillingness to participate.

Design outcomes

Primary

MeasureTime frame
Proportion of patients with adequate standards of bowel preparation;

Secondary

MeasureTime frame
BBPS score;Cecal intubation time;Polyp detection rate (PDR);Adenoma Detection Rate (ADR);

Countries

China

Contacts

Public ContactXiuli Zuo

Qilu Hospital of Shandong University

zuoxiuli@sdu.edu.cn+86 185 6008 0066

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026