Renal Nerve Denervation in Patients With Hypertension and Paroxysmal and Persistent Atrial Fibrillation
- Disease/Condition
- Atrial Fibrillation,Hypertension
- Drug/Device/Intervention
- Symplicity Spyral™ Multi-Electrode Renal Denervation Catheter
- Study type
- Interventional
- Intervention type
- device
- Primary sponsor
- Medtronic Vascular
- Location
- Sacramento,Burlington,Marquette,New York,Columbus,Doylestown,Pittsburgh,Seattle,Seattle,Homburg, Germany,United States of America
- Phase
- N/A
- Start date
- Feb 01, 2015
- End date
- Apr 19, 2021
- Enrollment
- 102 participants
Safety composite events,Rate of chronic treatment success between study arms
The purpose of this clinical study is to evaluate the feasibility of performing both renal
 nerve denervation and pulmonary vein isolation on the same patient with the intent of
 characterizing both safety and effectiveness in a paroxysmal and persistent atrial
 fibrillation population with hypertension. To assess safety, the study will measure the
 occurrence of a composite safety endpoint and, to assess effectiveness, the study will
 measure freedom of chronic treatment failure through a minimum of six months of follow-up.
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT02064764
- Type
- Device Trial
Access comprehensive clinical trial information for NCT02064764 through Pure Global AI's free database. This phase not specified trial is sponsored by Medtronic Vascular and is currently Completed. The study focuses on Atrial Fibrillation,Hypertension. Target enrollment is 102 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.