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Difference Analysis of Colonoscopy Detection Rate of Adenoma Assisted by Artificial Intelligence

Difference Analysis of Colonoscopy Detection Rate of Adenoma Assisted by Artificial Intelligence

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000034887
Enrollment
Unknown
Registered
2020-07-23
Start date
2020-07-22
Completion date
Unknown
Last updated
2020-07-27

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

Conditions

Adenoma of colon

Interventions

Experimental group:colonoscopy with artificial intelligence
control group:conventional colonoscopy

Sponsors

Xuchang Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Male or female over 18 years old; 2. Those who need enteroscopy to further clarify the characteristics of digestive tract diseases; 3. No contraindications for colonoscopy; 4. Those who agree to have painless colonoscopy; 5. Those who can read, understand and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with contraindications of colonoscopy; 2. Anesthesiologists assessed that subjects were not suitable for painless colonoscopy; 3. Patients with previous history of colorectal cancer; 4. Patients with contraindication of biopsy; 5. Patients with known active lower gastrointestinal bleeding or emergency colonoscopy; 6. Pregnant women; 7. Patients with previous intestinal resection history; 8. High risk diseases or other special conditions considered by the researchers to be unsuitable for clinical trials.

Design outcomes

Primary

MeasureTime frame
adenoma detection rate;

Countries

China

Contacts

Public ContactDuan Shufen

Xuchang Central Hospital

1028745636@qq.com+86 15537423878

Outcome results

None listed

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