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The Impact of a Colonoscopy Monitoring Program on Endoscopists' Performance

Not Applicable
Not yet recruiting
Conditions
Adenoma Colon Polyp
Sessile Serrated Adenoma
Interventions
Behavioral: Feedback from colonoscopy monitoring program
Registration Number
NCT06577610
Lead Sponsor
Seoul National University Hospital
Brief Summary

The goal of this clinical trial is to learn if colonoscopy monitoring program works to adenoma detection rate in endoscopists. It will also learn about the impact on sessile serrated lesion detection rate, adenomas per colonoscopy, sessile serrated lesions per colonoscopy, advanced adenoma detection rate. The main questions it aims to answer are:

Does colonoscopy monitoring program effect on adenoma detection rate in endoscopists?

Participants will:

Receive result of colonoscopy monitoring program or not every 3 months for 1 year

Detailed Description

Not available

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
16
Inclusion Criteria
  • Endoscopists with at least 1 year of colonoscopy experience
Exclusion Criteria
  • Endoscopists with less than 1 year of colonoscopy experience

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Feedback groupFeedback from colonoscopy monitoring programThe feedback group will be notified of the colonoscopy performances.
Primary Outcome Measures
NameTimeMethod
adenoma detection rate1 year

the percentage of patients with at least one histologically proven adenoma

Secondary Outcome Measures
NameTimeMethod
advanced adenoma detection rate1 year

the percentage of patients with at least one histologically proven advanced adenoma

sessile serrated lesions per colonoscopy1 year

the number of detected sessile serrated lesions divided by the total number of screening colonoscopies

adenomas per colonoscopy1 year

the number of detected adenomas divided by the total number of screening colonoscopies

sessile serrated lesion detection rate1 year

the percentage of patients with at least one histologically proven sessile serrated lesion

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