Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06676930

Impact of Artificial Intelligence on Trainee Polyp Miss Rates

Led by Northwestern University · Updated on 2024-11-06

180

Participants Needed

1

Research Sites

103 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Based on prior studies, trainee and practicing gastroenterologists miss pre-cancerous polyps (adenomas and serrated polyps) during colonoscopy. The use of computer-aided detection (CADe) systems, a form of artificial intelligence (AI) has been shown to help identify colorectal lesions for practicing gastroenterologists. However, less is known how AI impacts polyp detection for trainees. The investigators are conducting a tandem colonoscopy study wherein a portion of the colon is examined first by the trainee and then the attending physician. For each procedure, randomization will occur which will determine whether or not the trainee will utilize AI for their examination of the colon. At the end of the study, the investigators will determine whether AI helps trainees miss fewer polyps during colonoscopy. The investigators will also conduct interviews with trainees to understand how AI impacts colonoscopy training.

CONDITIONS

Official Title

Impact of Artificial Intelligence on Trainee Polyp Miss Rates

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients referred for screening or surveillance colonoscopy
Not Eligible

You will not qualify if you...

  • Patients referred for polypectomy or diagnostic colonoscopy
  • Patients with prior right colon surgery
  • Prolonged insertion time (greater than 20 minutes)
  • Poor bowel preparation (Boston Bowel Preparation Score less than or equal to 6)

AI-Screening

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Trial Site Locations

Total: 1 location

1

Northwestern Memorial Hospital

Chicago, Illinois, United States, 60611

Actively Recruiting

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Research Team

R

Rajesh Keswani, MD

CONTACT

Z

Zack Jacob

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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