RecruitingNCT02989818

Multi-center Evaluation of the Clinical Utility of ESD in the Western Population

Multi-center Prospective Evaluation of the Clinical Utility of Endoscopic Submucosal Dissection (ESD) in the Western Population


Sponsor

University of Florida

Enrollment

300 participants

Start Date

Mar 1, 2016

Study Type

OBSERVATIONAL

Conditions

Summary

The aim of this multi-center study is to prospectively document the clinical utility of ESD.


Eligibility

Min Age: 18 YearsMax Age: 100 Years

Plain Language Summary

Simplified for easier understanding

This multi-centre study evaluates how endoscopic submucosal dissection (ESD) — a minimally invasive procedure to remove early-stage gastrointestinal tumours from the lining of the gut — is performed and what outcomes it achieves in Western healthcare settings. This helps determine whether ESD is as effective in Western populations as it is in Asian populations where it was first developed. You may be eligible if: - You are 18 years of age or older - You are already scheduled to undergo ESD as part of your standard medical care You may NOT be eligible if: - You have a contraindication to endoscopy - You are participating in another research study that could affect the results - You are unable or unwilling to provide informed consent Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHEREndoscopic Submucosal Dissection

This intervention is part of the subjects standard of care and is a method to remove the Gastrointestinal lesion.


Locations(3)

University of Florida

Gainesville, Florida, United States

Massachusetts General Hospital

Boston, Massachusetts, United States

Baylor College of Medicine

Houston, Texas, United States

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NCT02989818


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