Patient Registry: Radio Frequency Ablation of Barrett's Esophagus Using HALO System
- Conditions
- Barrett's Esophagus
- Registration Number
- NCT02033070
- Lead Sponsor
- Ochsner Health System
- Brief Summary
The purpose of this study is to provide a tool for physicians to compare outcome data related to the use of the HALO Ablation Systems. This study is a single-center patient registry which will contribute to a framework for treatment and follow-up of patients with Barrett's Esophagus.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- Not specified
Inclusion Criteria
- candidate for ablation of Barrett's Esophagus with the HALO Ablation System (Prospective)
- received an ablation with the HALO Ablation System to treat Barrett's Esophagus (Retrospective)
- candidate agrees to proposed follow-up schedule of yearly surveillance following treatment
- signs consent
Exclusion Criteria
- has not been diagnosed with Barrett's Esophagus
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Endoscopic clearance rate for Barrett's Esophagus Outcome measure is assessed at Month 12
- Secondary Outcome Measures
Name Time Method Histological clearance rate for intestinal metaplasia Biopsy taken at 12 months
Trial Locations
- Locations (1)
Ochsner Medical Center
🇺🇸Kenner, Louisiana, United States