Key result
This study is a protocol designed to evaluate the efficacy and safety of Zhen Wu Decoction for chronic heart failure, and no clinical results are reported.
Why the study?
Despite modern therapy, many patients with chronic heart failure suffer repeated hospitalization and side effects, prompting evaluation of Zhen Wu Decoction, a traditional prescription widely used in China.
Does Zhen Wu Decoction improve echocardiographic parameters, natriuretic peptides, and exercise capacity in patients with chronic heart failure?
RCT
Double-blind
1:1 ratio
Does Zhen Wu Decoction improve echocardiographic parameters, natriuretic peptides, and exercise capacity in patients with chronic heart failure?
Answers are grounded in this paper and cite their sources.
This study protocol outlines a randomized controlled trial to evaluate the efficacy and safety of Zhen Wu Decoction in patients with chronic heart failure.
INTRODUCTION: Chronic heart failure (CHF) is the end stage of several cardiac diseases. 50% of patients with severe CHF would survive less than 1 year, which has seriously affected patients' survival and quality of life. The current modern therapy could improve survival and quality of life. However, a larger number of patients still suffer from repeated hospitalization, unsatisfactory efficacy, and many side effects. In China, Zhen Wu Decoction (ZWD), a classic prescription recorded in Treatise on Febrile Diseases, was widely used for CHF. In this study, we try to conduct a prospective, double-blinded, randomized, controlled study to evaluate the efficacy and safety of ZWD in the treatment of CHF patients in China. METHODS: Patients will be randomly divided into treatment group and control group in 1:1 ratio. Guideline directed medical therapies and ZWD will be provided for patients in treatment group, while guideline directed medical therapies and ZWD-granules simulations for control group. Left ventricular ejection fraction, left ventricular end diastolic diameter, left ventricular end systolic diameter, b-type natriuretic peptide, NT-proBNP, peak VO2, VO2 maximum, exercise time, and walking distance will be recorded. The data will be analyzed by SPSS 22.0. CONCLUSIONS: The results will evaluate the efficacy and safety of ZWD in the treatment of CHF patients. TRIAL REGISTRATION: OSF registration number: DOI 10.17605/OSF.IO/G3QNU.
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Liang et al. (2021) conducted an RCT in Chronic heart failure (CHF). Zhen Wu Decoction (ZWD) vs. ZWD-granules simulations (placebo) was evaluated on Left ventricular ejection fraction, left ventricular end diastolic diameter, left ventricular end systolic diameter, b-type natriuretic peptide, NT-proBNP, peak VO2, VO2 maximum, exercise time, and walking distance. This study is a protocol designed to evaluate the efficacy and safety of Zhen Wu Decoction for chronic heart failure, and no clinical results are reported.
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