Observational Study of Endoscopic Submucosal Dissection (ESD)
This study is looking at Endoscopic Submucosal Dissection (ESD), a procedure used to remove growths in the digestive tract. It's an observational study, meaning researchers will collect information on patients already scheduled to have ESD as part of their regular medical care. The goal is to understand how well ESD works in Western populations, specifically by measuring the rate at which growths are removed in one piece (en-bloc resection). You may be able to join if you are 18 or older and are already scheduled for ESD. The study is currently unclear on its recruitment status and plans to enroll 300 participants.
- Study design
- This is a multi-center observational study aiming to enroll 300 participants. It is not a randomized or blinded study.
- What's involved
- You would receive standard medical care, and no experimental interventions will be performed. No additional studies or clinic visits are needed specifically for this study.
- Compensation
- Not stated in the trial record.
- Follow-up
- Follow-up will be carried out as medically indicated, not for a specific study duration. The primary endpoint is measured at 3-4 hours.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Multi-center Evaluation of the Clinical Utility of ESD in the Western Population
At a glance
Conditions
Where it's being run
3 sites across 3 statesStudy leadership
- Peter Draganov, MD · PRINCIPAL_INVESTIGATOR · University of Florida
Who to contact
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Do you actually qualify for this trial?
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Inclusion
Exclusion
What this trial measures
- Rate of en-bloc resection3-4 hours
An Excision of the targeted lesion in a single specimen