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Renal Nerve Denervation in Patients With Hypertension and Paroxysmal and Persistent Atrial Fibrillation - Trial NCT02064764

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.

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NCT02064764
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Trial Details
ClinicalTrials.gov โ€ข NCT02064764
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Renal Nerve Denervation in Patients With Hypertension and Paroxysmal and Persistent Atrial Fibrillation

Study Focus

Symplicity Spyralโ„ข Multi-Electrode Renal Denervation Catheter

Interventional

device

Sponsor & Location

Medtronic Vascular

Sacramento,Burlington,Marquette,New York,Columbus,Doylestown,Pittsburgh,Seattle,Seattle,Homburg, Germany,United States of America

Timeline & Enrollment

N/A

Feb 01, 2015

Apr 19, 2021

102 participants

Primary Outcome

Safety composite events,Rate of chronic treatment success between study arms

Summary

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.

ICD-10 Classifications

Chronic atrial fibrillation
Persistent atrial fibrillation
Paroxysmal atrial fibrillation
Atrial fibrillation and flutter
Atrial fibrillation and atrial flutter, unspecified

Data Source

ClinicalTrials.gov

NCT02064764

Device Trial