Outcomes of Disposable Distal Attachment Device (Endocuff and Transparent Plastic Cap) Assisted Colonoscopy

Withdrawn before enrolling · Not applicable

Conditions studied: Colorectal Neoplasms

In brief

The purpose of the study is to compare the efficacy of device assisted colonoscopy (DAC) with standard colonoscopy (SC) in detecting adenomas in a randomized fashion.

Key facts

Study ID

NCT02504411

Run by

The University of Texas Health Science Center, Houston

People needed

0

Starts

2015-08-01

Expected to finish

2017-02-15

Last updated by the study team

2018-08-13

Who can join

Age: 18 and older, up to 100. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Patients undergoing first screening colonoscopy
• Patients undergoing subsequent surveillance colonoscopies with known history of prior colon polyps detected on prior screening colonoscopies.
• Ability to provide informed consent.

You may not qualify if…

• Previous surgical resection of any part of the colon
• history of colon cancer
• history of inflammatory bowel disease
• use of antiplatelet agents or anti-coagulants that precluded removal of polyps
• Poor general condition
• History of polyposis syndrome or hereditary nonpolyposis colorectal cancer
• Inability to give informed consent.

Where it is running

• The University of Texas Health Science Center at Houston — Houston, Texas, United States

Full record on ClinicalTrials.gov

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