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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03637712
Other study ID # 18-00746
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 1, 2018
Est. completion date July 7, 2019

Study information

Verified date May 2020
Source NYU Langone Health
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The primary objective of this study is to examine the role of machine learning and computer aided diagnostics in automatic polyp detection and to determine whether a combination of colonoscopy and an automatic polyp detection software is a feasible way to increase adenoma detection rate compared to standard colonoscopy.


Recruitment information / eligibility

Status Completed
Enrollment 5
Est. completion date July 7, 2019
Est. primary completion date July 7, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 99 Years
Eligibility Inclusion Criteria:

- Patients presenting for routine colonoscopy for screening and/or surveillance purposes.

- Ability to provide written, informed consent and understand the responsibilities of trial participation

Exclusion Criteria:

- People with diminished cognitive capacity.

- The subject is pregnant or planning a pregnancy during the study period.

- Patients undergoing diagnostic colonoscopy (e.g. as an evaluation for active GI bleed)

- Patients with incomplete colonoscopies (those where endoscopists did not successfully intubate the cecum due to technical difficulties or poor bowel preparation)

- Patients that have standard contraindications to colonoscopy in general (e.g. documented acute diverticulitis, fulminant colitis and known or suspected perforation).

- Patients with inflammatory bowel disease

- Patients with any polypoid/ulcerated lesion > 20mm concerning for invasive cancer on endoscopy.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Computer Algorithm
This device is a computer algorithm that runs in the background during routine screening or surveillance colonoscopy that is designed to aid in the detection of polyps

Locations

Country Name City State
United States NYU Langone Health New York New York

Sponsors (1)

Lead Sponsor Collaborator
NYU Langone Health

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Adenoma Detection Rate the proportion of colonoscopic examinations performed that detect one or more polyp 1 Day
See also
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Completed NCT04838951 - Effect of Real-time Computer-aided System (ENDO-AID) on Adenoma Detection in Endoscopist-in-training N/A