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Clinical Trials/NCT01238913
NCT01238913
Withdrawn
N/A

Prospective Evaluation of the Clinical Utility of the Endoscopic Placement of Mental Stent for Benign Esophageal Lesions

University of Florida0 sitesSeptember 2015
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ConditionsBenign Esophageal Lesions

Overview

Phase
N/A
Intervention
Not specified
Conditions
Benign Esophageal Lesions
Sponsor
University of Florida
Primary Endpoint
Successful stenting of Benign esophageal lesions
Status
Withdrawn
Last Updated
10 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

The evaluation of using metal stents as medically indicated for the treatment of benign esophageal lesions.

Registry
clinicaltrials.gov
Start Date
September 2015
End Date
September 2015
Last Updated
10 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • •Subject is 18 years or older
  • •Subject has medical indication to undergo endoscopic placement of esophageal metal stent
  • •Subject must be able to give informed consent

Exclusion Criteria

  • •Any contraindications for endoscopic placement of esophageal metal stent
  • •The subject is unable to give informed consent.

Outcomes

Primary Outcomes

Successful stenting of Benign esophageal lesions

Time Frame: approximately 2-3 hours

This is an observational study to determine the effectiveness of stenting benign esophageal lesions with a metal stent.

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