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Spots Global Cancer Trial Database for Comparison of Adenoma Detection Rate With ENDOCUFF VISION® vs. G-EYE®

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Comparison of Adenoma Detection Rate With ENDOCUFF VISION® vs. G-EYE®

Official Title: A Prospective Randomized Comparison of Colonoscopy Adenoma Detection Rate With a Disposable Cap (ENDOCUFF VISION®) (Endocuff) Versus a Permanently Mounted Balloon (G-EYE®)

Study ID: NCT04708951

Study Description

Brief Summary: The study is intended to compare the detection rate obtained by performing G-EYE® high definition colonoscopy vs. the detection rate obtained by performing ECV high definition colonoscopy.

Detailed Description: This is a multicenter, two-arm, randomized, open-label study intended to compare the detection rate obtained by performing G-EYE® high definition colonoscopy vs. the detection rate obtained by performing ECV high definition colonoscopy.

Eligibility

Minimum Age:

Eligible Ages: CHILD, ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: Yes

Locations

IU Health University Hospital, Indianapolis, Indiana, United States

NYU Langone Health, New York, New York, United States

Helios Dr. Horst Schmidt Kliniken Wiesbaden, Wiesbaden, , Germany

Contact Details

Name: Ralf Kiesslich, Prof.

Affiliation: Helios Dr. Horst Schmidt Kliniken Wiesbaden

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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