Multi-center Prospective Registry Study Utilizing a Double Balloon Accessory Device to Facilitate Endoscopic Polypectomy in Large Intestine.

Status: Active, not recruiting
Location: See all (3) locations...
Intervention Type: Device
Study Type: Observational [Patient Registry]
SUMMARY

This study is collecting standard of care information pertaining to the use of the accessory device and patient outcomes when this double balloon accessory device is used during endoscopic procedures in the colon.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: No
View:

• Patients scheduled for endoscopic removal of suspected adenomatous benign polyps(s)

• Patients capable of giving informed consent in English

• No medical contraindication to endoscopic mucosal resection or endoscopic submucosal disection

Locations
United States
Florida
University of Florida - Division of Gastroenterology, Hepatology and Nutrition
Gainesville
Pennsylvania
Geisinger Health System
Danville
Texas
Baylor College of Medicine
Houston
Time Frame
Start Date: January 22, 2019
Estimated Completion Date: March 31, 2021
Participants
Target number of participants: 165
Sponsors
Leads: Lumendi, LLC

This content was sourced from clinicaltrials.gov

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