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松龄血脉康胶囊治疗中低危高血压患者的随机对照试验研究方案。

Songling Xuemaikang capsules for patients with low-to-medium risk hypertension: study protocol for a randomized controlled trial.

机构信息

Cardiovascular Disease Center, Xiyuan Hospital of China Academy of Chinese Medical Sciences, Beijing, 100091, China.

Graduate School of China Academy of Chinese Medical Sciences, 16 Nanxiaojie, Dongzhimen Nei, Beijing, 100700, China.

出版信息

Trials. 2019 Apr 15;20(1):218. doi: 10.1186/s13063-019-3308-5.

Abstract

BACKGROUND

Hypertension is a major risk factor for cardio-cerebrovascular disease. Songling Xuemaikang capsules (SXC), a formulation of Chinese herbal patent medicine, has been used as a complementary medicine with conventional western medicine to treat patients with hypertension since 1994 in mainland China. However, the efficacy of treatment with SXC alone against hypertension remains unclear.

METHODS/DESIGN: This is a multicenter, placebo-controlled, double-blinded, randomized controlled clinical trial. A total of 570 patients with low-to-medium risk hypertension are randomized in a 1:1 ratio to receive SXC or placebo three times daily for eight weeks. The primary outcomes are 24-h average systolic blood pressure and average diastolic blood pressure. The secondary outcomes are daytime average blood pressure, night-time average blood pressure, fluctuation of blood pressure, hypertension control rate, traditional Chinese medicine (TCM) syndrome scores, and quality-of-life scores.

DISCUSSION

This is the first multicenter trial conducted to evaluate the efficacy and safety of TCM in patients with low-to-medium risk hypertension. Our study will provide evidence-based results of a complementary preventive measure for hypertension.

TRIAL REGISTRATION

Chinese Clinical Trial Registry, ChiCTR-IPR-17011383 . Registered on 12 May 2017.

摘要

背景

高血压是心脑血管疾病的主要危险因素。松龄血脉康胶囊(SXC)是一种中药专利药配方,自 1994 年以来,在中国内地一直被用作与常规西药联合治疗高血压患者的辅助药物。然而,单独使用 SXC 治疗高血压的疗效尚不清楚。

方法/设计:这是一项多中心、安慰剂对照、双盲、随机对照临床试验。共有 570 例中低危高血压患者以 1:1 的比例随机分为 SXC 组或安慰剂组,每天 3 次,连续 8 周。主要结局是 24 小时平均收缩压和平均舒张压。次要结局是白天平均血压、夜间平均血压、血压波动、高血压控制率、中医(TCM)证候评分和生活质量评分。

讨论

这是首次评估中低危高血压患者中药疗效和安全性的多中心试验。我们的研究将为高血压的辅助预防措施提供基于证据的结果。

试验注册

中国临床试验注册中心,ChiCTR-IPR-17011383。于 2017 年 5 月 12 日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0694/6466697/b7c859dc558a/13063_2019_3308_Fig1_HTML.jpg

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