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Spots Global Cancer Trial Database for Endocuff-assisted Versus Cap-assisted Versus Standard Colonoscopy

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Trial Identification

Brief Title: Endocuff-assisted Versus Cap-assisted Versus Standard Colonoscopy

Official Title: Endocuff-assisted Versus Cap-assisted Versus Standard Colonoscopy for Adenoma Detection: A Randomized Controlled European Multicenter Study

Study ID: NCT02331836

Study Description

Brief Summary: Comparison of Endocuff-assisted, Cap-assisted and Standard colonoscopy for assessment of the adenoma detection rate (ADR)

Detailed Description: The Endocuff is a medical device, approved in 2012 by the American Food and Drug Administration, which was also authorized by the European Agency for the Evaluation of Medicinal Products. The aim of the cuff is to optimize the view of the colonic mucosa. There is also a transparent cap on the market, which is used in colonoscopy for a better evaluation of the mucosa and polyp detection. The goal of this project is to conduct a prospective randomized trial for clarification of the hypotheses, whether the usage of the Endocuff increases the detection rate of adenomas compared to the transparent cap or compared to standard colonoscopy.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

University of Muenster, Muenster, North-Rhine Westphalia, Germany

University Medical Center Göttingen, Göttingen, , Germany

HELIOS St. Marienberg Klinik Helmstedt, Helmstedt, , Germany

HELIOS Albert-Schweitzer-Klinik, Northeim, , Germany

HELIOS Medical Center Siegburg, Siegburg, , Germany

Wroclaw Medical University, Wroclaw, , Poland

Contact Details

Name: Tobias Meister, Prof. Dr.med.

Affiliation: Helios Albert-Schweitzer-Hospital

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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