Benign Esophageal Lesions Clinical Trial
Official title:
Prospective Evaluation of the Clinical Utility of the Endoscopic Placement of Mental Stent for Benign Esophageal Lesions
| Verified date | September 2015 |
| Source | University of Florida |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | United States: Institutional Review Board |
| Study type | Observational |
The evaluation of using metal stents as medically indicated for the treatment of benign esophageal lesions.
| Status | Withdrawn |
| Enrollment | 0 |
| Est. completion date | September 2015 |
| Est. primary completion date | September 2015 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: 1. Subject is 18 years or older 2. Subject has medical indication to undergo endoscopic placement of esophageal metal stent 3. Subject must be able to give informed consent Exclusion Criteria: 1. Any contraindications for endoscopic placement of esophageal metal stent 2. The subject is unable to give informed consent. |
Observational Model: Case-Only, Time Perspective: Prospective
| Country | Name | City | State |
|---|---|---|---|
| n/a | |||
| Lead Sponsor | Collaborator |
|---|---|
| University of Florida |
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Successful stenting of Benign esophageal lesions | This is an observational study to determine the effectiveness of stenting benign esophageal lesions with a metal stent. | approximately 2-3 hours | No |
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT01337206 -
SX ELLA Esophageal Degradable BD Stent System
|
N/A |