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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03622281
Other study ID # 2018SDU-QILU-716
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 20, 2018
Est. completion date May 31, 2019

Study information

Verified date February 2020
Source Shandong University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Quality measures in colonoscopy are important guides for improving the quality of patient care. But quality improvement intervention is not taking place, primarily because of the inconvenience and expense. To address the difficulties above, we used artificial intelligence for quality control of colonoscopy.


Recruitment information / eligibility

Status Completed
Enrollment 676
Est. completion date May 31, 2019
Est. primary completion date May 31, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- aged between 18 and 80;

- agree to give written informed consent.

Exclusion Criteria:

- patients with the contraindications to colonoscopy examination;

- patients with a history of inflammatory bowel disease (IBD), CRC, colorectal surgery;

- patients with prior failed colonoscopy and high suspicion of polyposis syndromes, IBD and typical advanced CRC;

- patients refused to participate in the trial;

- the colonoscopyprocedure cannot be completed due to stenosis, obstruction, huge occupying lesions, or solid stool;

- the colonoscopy procedure have to be terminated due to complications of anaesthesia.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
quality improvement intervention using artificial intelligence
Colonoscopists received performance measure monitoring and feedback

Locations

Country Name City State
China Department of Gastroenterology, Qilu Hospital, Shandong University Jinan Shandong

Sponsors (1)

Lead Sponsor Collaborator
Shandong University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Adenoma detection rate Adenoma detection rate was defined as the number of exams with findings of adenoma divided by the total number of exams. 8 months
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