Evaluation of the DiLumen Device During Colonoscopy

Completed

Conditions studied: Colon Polyp

In brief

This is an observational registry study collecting data on the clinical performance of the study device (DiLumen™ ) for its intended use. The primary objective is to evaluate functional outcomes of the DiLumen device in humans. The secondary objective is to evaluate safety characteristics of the DiLumen device.

Key facts

Study ID

NCT03113578

Run by

Lumendi, LLC

People needed

30

Starts

2017-04-26

Expected to finish

2017-09-27

Last updated by the study team

2017-12-02

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients listed for routine surveillance colonoscopy for colorectal cancer and capable of giving informed consent

You may not qualify if…

• No patients less than 18 years of age.
• Any contraindication to routine surveillance colonoscopy
• History of open or laparoscopic colorectal surgery
• History of Inflammatory Bowel Disease

Where it is running

• New York Presbyterian Hospital — New York, New York, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.