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Vagus Nerve Injury Post Radiofrequency Catheter Ablation for Atrial Fibrillation

Atrial Fibrillation Clinical Trial

Official title:
Vagus Nerve Injury Post Radiofrequency Catheter Ablation for Atrial Fibrillation (Vagus Nerve Study)

Clinical Trial 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.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02562404
Study type Observational
Source Intermountain Health Care, Inc.
Contact
Status Completed
Phase N/A
Start date April 2015
Completion date December 2016
View Details
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