Clinical trial · Observational
Patient Registry: Radio Frequency Ablation of Barrett's Esophagus Using HALO System
Single Center Patient Registry Using Radio Frequency Ablation of Barrett's Esophagus Using HALO System
NCT02033070CI-TRIAL-00013390HALOunknownClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Barrett's Esophagus | — | UNRESOLVED | — |
Interventions
Interventions (0)
Data not yet available
No intervention recorded.
Design
Arms and outcomes
Arms (1)
- label
- Non-Dysplastic IM, LGD, HGD
Primary outcomes (1)
- measure
- Endoscopic clearance rate for Barrett's Esophagus
- timeFrame
- Outcome measure is assessed at Month 12
Secondary outcomes (1)
- measure
- Histological clearance rate for intestinal metaplasia
- timeFrame
- Biopsy taken at 12 months
Eligibility
Eligibility (as posted)
- Sex
- All
Show eligibility criteria text
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
References
Publications (0)
Data not yet available
No reference posted for this study.