Trials / Completed
CompletedNCT02562404
Vagus Nerve Injury Post Radiofrequency Catheter Ablation for Atrial Fibrillation
Vagus Nerve Injury Post Radiofrequency Catheter Ablation for Atrial Fibrillation (Vagus Nerve Study)
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 100 (actual)
- Sponsor
- Intermountain Health Care, Inc. · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study is an observational study designed to determine the extent of gastrointestinal (GI) post-procedure complications after Radiofrequency Catheter Ablation (RFCA) for atrial fibrillation (AF). This exploratory study will evaluate patient symptoms prior to the RFCA procedure, at 1 month post RFCA procedure, and at 3 months post RFCA procedure, through the administration of a questionnaire. The purpose of this study is to determine if vagus nerve injury resulting from RFCA for AF increases the risk of post-procedure GI complications that may present as temporary or permanent symptoms.
Conditions
Timeline
- Start date
- 2015-04-01
- Primary completion
- 2016-09-01
- Completion
- 2016-12-01
- First posted
- 2015-09-29
- Last updated
- 2017-03-03
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT02562404. Inclusion in this directory is not an endorsement.