Post-resection Treatment of Large Colon Polyps

Completed · Not applicable

Conditions studied: Recurrence

In brief

Patients who have provided informed consented and are scheduled to undergo endoscopic mucosal resection (EMR) of lesions 15mm and larger will be randomized to STSC (80 W, Effect 5) vs APC (preferred settings) vs No Treatment of the perimeter of the EMR site.

Key facts

Study ID

NCT03654209

Run by

Indiana University

People needed

384

Starts

2018-10-16

Expected to finish

2022-12-14

Last updated by the study team

2024-01-05

Who can join

Age: 25 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 25 years and older
• Ability to provide informed consent
• Undergoing colonoscopy for screening, surveillance, diagnostic reasons, or removal of a lesion

You may not qualify if…

• Pedunculated lesions
• Inflammatory bowel disease
• Inability to provide informed consent
• Lesions less than 15mm in largest dimension

Where it is running

• Sibley Memorial Hospital — Washington D.C., District of Columbia, United States
• AdventHealth Orlando — Orlando, Florida, United States
• Indiana University Health University Hospital — Indianapolis, Indiana, United States
• Spring Mill Medical Center — Indianapolis, Indiana, United States
• The University of Kansas Medical Center — Kansas City, Kansas, United States
• The Johns Hopkins Hospital — Baltimore, Maryland, United States
• Dartmouth-Hitchcock Medical Center — Lebanon, New Hampshire, United States
• NYU Langone Medical Center — New York, New York, United States
• The Mount Sinai Hospital — New York, New York, United States
• Penn State Health Milton S. Hershey Medical Center — Hershey, Pennsylvania, United States

Full record on ClinicalTrials.gov

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