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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04901130
Other study ID # 2021SDU-QILU-066
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date May 27, 2021
Est. completion date January 31, 2022

Study information

Verified date May 2021
Source Shandong University
Contact Zhen Li, PhD
Phone 18560086106
Email lizhenh@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study was to assess the performance of automatic quality-control system (AQCS) in real-time quality control of colonoscopy.


Description:

We carried a multicenter randomised controlled trial to assess the performance of this system in quality control of real-time colonoscopy, including the adenoma detection rate (ADR), withdraw time, adequate bowel preparation rate and other indicators.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 1254
Est. completion date January 31, 2022
Est. primary completion date January 1, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Consecutive patients (aged 18-80 years) scheduled for colonoscopy examination. Exclusion Criteria: - Patients with a history of inflammatory bowel disease, advanced colorectal cancer, polyposis syndromes or known colorectal polyps without complete removal previously. - Patients with a history of colorectal surgery. - Patients with a contraindication for biopsy. - Patients with prior failed colonoscopy. - Patients with known stenosis or obstruction. - Patients in pregnancy or lactation phase. - Patients refused to participate in the trial.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Computer-aided Real-time Automatic Quality Control System (AQCS)
Automatic quality-control system(AQCS), developed based on deep convolutional neural network (DCNN) models, could improve the colonoscopists' performance during withdrawal phase and significantly increase polyp and adenoma detection.

Locations

Country Name City State
China Binzhou Medical University Hospital Binzhou Shandong
China Linyi People's Hospital Dezhou Shandong
China Central Hospital of Shengli Oilfield Dongying Shandong
China Qilu Hospital of Shandong University Jinan Shandong
China The People's Hospital of Zhaoyuan City Yantai Shandong
China Zibo Municipal Hospital Zibo Shandong

Sponsors (6)

Lead Sponsor Collaborator
Shandong University Binzhou Medical University, Central Hospital of Shengli Oilfield, Linyi People's Hospital, The People's Hospital of Zhaoyuan City, Zibo municipal hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Colorectal adenoma detection rate (ADR) The primary endpoint is the adenoma detection rate (ADR), which is the proportion of patients having one or more adenomas detected by colonoscopy. 10 months
Secondary Colorectal polyp detection rate (PDR) The polyp detection rate (PDR) is the proportion of patients having one or more polyps detected by colonoscopy. 10 months
Secondary The mean number of adenomas detected per colonoscopy (APC) The mean number of adenomas detected per colonoscopy in AQCS and control groups 10 months
Secondary The mean number of polyps detected per colonoscopy (PPC) The mean number of polyps detected per colonoscopy in AQCS and control groups 10months
Secondary Withdrawl time Withdrawl time is defined as the time taken to remove the colonoscope from the cecal pole minus the time of therapeutic interventions or biopsy, until the complete withdrawal of the colonoscope. During procedure
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