Endoscopic Quality Improvement System Study

Renmin Hospital of Wuhan University17 enrolled

Overview

We intend to develop intelligent quality control and management software based on the work of digestive endoscopic artificial intelligence in the Department of Gastroenterology, Wuhan University Renmin Hospital, to accurately and comprehensively assess the quality of gastrointestinal endoscopy and to provide a practical basis for improving the quality of digestive endoscopy in our endoscopic center.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

HEALTH_SERVICES_RESEARCH

Masking

SINGLE

Enrollment

Conditions

Adenoma Colon Gastric Precancerous Condition

Interventions

Quality audit and feedbackBEHAVIORAL

Endoscopists received quality report generated by Endo.Adm.

ControlBEHAVIORAL

None feedback.

Eligibility

Sex: ALLMin age: 18 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: Endoscopist: 1. Endoscopist with more than one year experience in gastrointestinal mirror operation; 2. Willing to further improve endoscopic quality through Endo.Adm feedback; 3. Ability to read, understand and sign informed consent; The investigator believes that the subject understands the flow of the clinical study and is willing and able to complete all research procedures and follow-up visits in conjunction with the research process. Exclusion Criteria: Endoscopist: 1. Have participated in other clinical trials; 2. Frequently attending in academic conference which is difficult to ensure the number of endoscopic operations; 3. Endoscopist who were either not present for both parts (phase1 and phase2) of the study. Patients: Colonoscopy: 1. Polyposis syndromes 2. Lumen obstruction 3. History of colorectal surgery 4. History of colorectal surgery Gastroscopy: 1. Obstruction 2. History of gastric surgery

Locations (1)

Renmin Hospital of Wuhan University

Wuhan, Hubei, China

Outcomes

Primary Outcomes

Adenoma detection rate

ADR was calculated by dividing the total number of patients being detected adenomas by the number of colonoscopies.

Time frame: 3 Months

Gastric precancerous detection rate

GPCs detection rate was calculated by dividing the total number of patients being detected gastric precancerous by the number of gastroscopies.

Time frame: 3 Months

Secondary Outcomes

Adcanced ADR

Adcanced ADR was calculated by dividing the total number of patients being detected ≥10mm in size, or adenomas with histopathology of tubulovillous, villous, adenocarcinoma, or high-grade dysplasia by the number of colonoscopies.

Time frame: 3 months

Data from ClinicalTrials.gov

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