Colon Cancer Clinical Trial

Standard Colonoscopy Versus Colonoscopy With Endocuff Vision

Summary

This study seeks to compare colonoscopy results between a standard method and one using a distal scope attachment (Endocuff Vision).

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Full Description

For this study, subjects will be randomized into one of two groups (those who receive a standard colonoscopy and those who receive a colonoscopy with an Endocuff Vision attachment). Results will then be compared between the two; these include insertion time (time it takes to reach the cecum of the large intestine), inspection time (time spent examining the large intestine), the total time per each polypectomy (removal of polyps in the colon), and the total procedure time of the colonoscopy.

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Eligibility Criteria

Inclusion Criteria:

Subject referred for a screening or surveillance colonoscopy
Subject is aged 40 years or older
Subject has the ability to provide informed consent

Exclusion Criteria:

Prior history of colon cancer
History of inflammatory bowel disease
Prior surgical resection of any part of the colon
Use of antiplatelet agents or anticoagulants that precludes the removal of polyps during the procedure
History of polyposis syndrome or HNPCC
Family history of colon cancer in a first-degree relative < 60 years or two first degree relatives with colorectal cancer
Inability to provide informed consent

Study is for people with:

Colon Cancer

Estimated Enrollment:

200

Study ID:

NCT03361917

Recruitment Status:

Completed

Sponsor:

Indiana University

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There is 1 Location for this study

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Indiana University
Indianapolis Indiana, 46202, United States

How clear is this clinincal trial information?

Study is for people with:

Colon Cancer

Estimated Enrollment:

200

Study ID:

NCT03361917

Recruitment Status:

Completed

Sponsor:


Indiana University

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