期刊论文详细信息
Trials
Renal sympathetic denervation versus antiarrhythmic drugs for drug-resistant hypertension and symptomatic atrial fibrillation (RSDforAF) trial: study protocol for a randomized controlled trial
Qijun Shan1  Yuehui Yin2  Min Qiu1 
[1] Cardiovascular Department, The First Affiliated Hospital of Nanjing Medical University, No 300, Guangzhou Road, Nanjing, Jiangsu 210029, China;Cardiovascular Department, The Second Affiliated Hospital of Chongqing Medical University, No 76, Linjiang Road, Chongqing, China
关键词: Clinical trial;    Sympathetic nerve;    Atrial fibrillation;    Hypertension;    Renal sympathetic denervation;   
Others  :  1093752
DOI  :  10.1186/1745-6215-14-168
 received in 2013-02-18, accepted in 2013-05-28,  发布年份 2013
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【 摘 要 】

Background

Recently, catheter-based renal sympathetic denervation (RSD) has been verified to be safely used to substantially reduce the levels of blood pressure, left ventricular hypertrophy, sleep apnea severity and norepinephrine spillover, and improve glucose tolerance. All these pathological changes are recognized as independent risk factors for the development and recurrence of atrial fibrillation (AF). A randomized, single-blind, parallel-control, multicenter clinical trial is being conducted to compare RSD with antiarrhythmic drugs (AAD) in patients with drug-resistant hypertension and symptomatic AF (RSDforAF trial).

Methods/design

Patients with drug-resistant hypertension and symptomatic AF will be randomized to RSD and the drug treatment groups. Patients will be followed for 12 months until study closure. Up to 200 patients may be enrolled in six medical centers in China. The primary objective is to study the effects of RSD on AF burden and blood pressure in patients with hypertension and symptomatic AF.

Discussion

RSDforAF trial will test the hypothesis that RSD is superior to AAD in reducing AF burden and blood pressure in patients with drug-resistant hypertension and symptomatic AF.

Trial registration

ClinicalTrials.gov, NCT01713270

【 授权许可】

   
2013 Qiu et al.; licensee BioMed Central Ltd.

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