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

Part of paid clinical trials in Gainesville, Florida.

Sponsor
University of Florida
Study ID
NCT02989818
Status
Recruiting
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Conditions

  • Endoscopic Submucosal Dissection

Eligibility Criteria

Sex
ALL
Age
18 Years - 100 Years
Healthy Volunteers
Not accepted

Interventions

  • Endoscopic Submucosal Dissection — OTHER
    This intervention is part of the subjects standard of care and is a method to remove the Gastrointestinal lesion.

Study Details

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

Key Dates

Start date
Mar 31, 2016
Status verified
Jun 2025
Primary completion
Jan 31, 2028
Completion
Jan 31, 2028

Study Design

Enrollment
300 participants (estimated)

Arms

  • Arm: Lesion of the Gastrointestinal tract
    Investigator will collect prospective data on the Endoscopic Submucosal dissection that is used as part of the subjects standard of care to remove the Gastrointestinal lesion

Primary Outcome Measure

Rate of en-bloc resection [ Time Frame: 3-4 hours ]

Central Contacts

Locations (3)

FacilityCityStateZIPSite coordinators
University of FloridaGainesvilleFlorida32610
Peter Draganov, MD
[email protected]
352-273-9472
Peter Draganov, MD (PRINCIPAL_INVESTIGATOR)
Massachusetts General HospitalBostonMassachusetts02114-
Baylor College of MedicineHoustonTexas77030-

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University of Florida· Gainesville, FLMassachusetts General Hospital· Boston, MABaylor College of Medicine· Houston, TX

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