Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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WITHDRAWN
OBSERVATIONAL
2015-09-30
2015-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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benign esophageal lesions
All patients who have a benign esophageal lesion where it is medically indicated that they receive a stent.
Endoscopy
Endoscopic placement of an esophageal metal stent as per medical indication.
Interventions
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Endoscopy
Endoscopic placement of an esophageal metal stent as per medical indication.
Eligibility Criteria
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Inclusion Criteria
2. Subject has medical indication to undergo endoscopic placement of esophageal metal stent
3. Subject must be able to give informed consent
Exclusion Criteria
2. The subject is unable to give informed consent.
18 Years
ALL
No
Sponsors
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University of Florida
OTHER
Responsible Party
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Principal Investigators
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Peter Draganov, MD
Role: PRINCIPAL_INVESTIGATOR
University of Florida
Other Identifiers
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Benign esophageal lesions
Identifier Type: -
Identifier Source: org_study_id
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