CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 1,382 enrolled
Drug / intervention
Endocuff groupprocedure
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03442738
NCT03442738N/ACompleted

A Prospective Randomized Comparison of the Adenoma Detection Rate in Screening Colonoscopy With and Without a Disposable Cap (ENDOCUFF VISION®)

Universitätsklinikum Hamburg-Eppendorf·observational·Posted Feb 22, 2018·Updated Jun 28, 2023

In Brief

An observational study evaluating Endocuff group for Adenoma Detection Rate. Completed, enrolled 1,382 participants across 9 sites.

Detailed Summary

The aim of this study is to evaluate the effect of ENDOCUFF VISION® (caps with soft, about 1 cm long lateral feet of rubber ("Endocuff") to flatten the colon folds) on ADR in a real-life setting (general practices) and in a homogenous patient collective (screening colonoscopies only). It is a prospective randomized multi centric study, with participation of at least 10 study sites (private practice). The study is an inverstigator-initiated trial (IIT). Depending on the randomization (closed envelope), the patients are examined with the standard instruments without or with ENDOCUFF VISION®. Group 1: screening colonoscopy with standard colonoscopes with ENDOCUFF VISION® Group 2: screening colonoscopy with standard colonoscopes without cap

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesGermany
CollaboratorsNorgine

Timeline

N/ACompletedFinished
201820192020202120222023202420252026
First PostedFeb 22, 2018
Enrollment StartSep 1, 2017
Primary CompletionSep 30, 2021
Study CompletionSep 30, 2022
TodayJul 2, 2026
Enrollment to primary: 4.1 yearsPosted 8.4 years ago

Interventions

Endocuff groupprocedure

Endocuff Vision cap on Standard colonoscope