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Patient Registry: Radio Frequency Ablation of Barrett's Esophagus Using HALO System

O

Ochsner Health System

Status

Unknown

Conditions

Barrett's Esophagus

Study type

Observational

Funder types

Other

Identifiers

NCT02033070
Barrett's RFA

Details and patient eligibility

About

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.

Sex

All

Volunteers

No Healthy Volunteers

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

Trial design

0 participants in 1 patient group

Non-Dysplastic IM, LGD, HGD

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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