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Efficacy and safety of Xinnaoning capsule in treating chronic stable angina (qi stagnation and blood stasis syndrome): Study protocol for a multicenter, randomized, double-blind, placebo-controlled trial.
Zhao, Jun-Nan; Zhang, Ying; Lan, Xu; Chen, Yao; Li, Jing; Zhang, Ping; Wu, Li-Qi; Jia, Shu-Ting; Liu, Yue; Xu, Feng-Qin.
Afiliação
  • Zhao JN; Institute of Geriatric Medicine, Xiyuan Hospital of China Academy of Chinese Medical Sciences.
  • Zhang Y; Institute of Geriatric Medicine, Xiyuan Hospital of China Academy of Chinese Medical Sciences.
  • Lan X; Institute of Geriatric Medicine, Xiyuan Hospital of China Academy of Chinese Medical Sciences.
  • Chen Y; Institute of Geriatric Medicine, Xiyuan Hospital of China Academy of Chinese Medical Sciences.
  • Li J; Institute of Geriatric Medicine, Xiyuan Hospital of China Academy of Chinese Medical Sciences.
  • Zhang P; Institute of Geriatric Medicine, Xiyuan Hospital of China Academy of Chinese Medical Sciences.
  • Wu LQ; Institute of Geriatric Medicine, Xiyuan Hospital of China Academy of Chinese Medical Sciences.
  • Jia ST; Beijing Duheng for Drug Evaluation and Research Co., Ltd.
  • Liu Y; Cardiovascular Diseases Center, Xiyuan Hospital of China Academy of Chinese Medical Sciences, Beijing, China.
  • Xu FQ; Institute of Geriatric Medicine, Xiyuan Hospital of China Academy of Chinese Medical Sciences.
Medicine (Baltimore) ; 98(31): e16539, 2019 Aug.
Article em En | MEDLINE | ID: mdl-31374015
ABSTRACT

BACKGROUND:

Chronic stable angina (CSA) is a cardiovascular disease with high prevalence. At present, drug treatment is still the main measure of stable angina pectoris. Traditional Chinese medicine has a long history in the treatment of CSA. Qi stagnation and Blood stasis syndrome is a common syndrome of CSA. Xinnaoning (XNN) capsule is considered as an effective adjuvant treatment for CSA with the efficacy of promoting qi and blood circulation but lack of high-quality clinical evidence. The purpose of this study is to evaluate the efficacy and safety of XNN capsule compared with placebo by clinical trial.

METHODS:

This multicenter, randomized, double-blind, placebo-controlled trial will be conducted with a total of 240 participants diagnosed with chronic stable angina (qi stagnation and blood stasis syndrome). The participants will be randomized (11) into groups receiving either XNN or placebo for 12 weeks. After a 2-week run-in period, they will receive either XNN or placebo (3 pills, 3 times daily) for 12 weeks on the basis of conventional therapy. The primary outcomes include changes in the integral scores of angina symptoms. The secondary outcome measures include changes in the total score of traditional Chinese medicine syndrome, severity grading of angina pectoris, the number of angina pectoris per week, nitroglycerin dosage, score of seattle angina scale, serum homocysteine, incidence of cardiovascular events. Safety outcomes will also be assessed. Adverse events will be monitored throughout the trial.

RESULTS:

This study will investigate whether XNN capsule can alleviate clinical symptoms, and improve quality of life of patients with chronic stable angina (qi stagnation and blood stasis syndrome). The results of this study will provide clinical evidence for the application of XNN capsule in the treatment of chronic stable angina. TRIAL REGISTRATION ClinicalTrials.gov NCT03914131.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Angina Estável Tipo de estudo: Clinical_trials / Diagnostic_studies / Risk_factors_studies Aspecto: Patient_preference Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Medicine (Baltimore) Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Angina Estável Tipo de estudo: Clinical_trials / Diagnostic_studies / Risk_factors_studies Aspecto: Patient_preference Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Medicine (Baltimore) Ano de publicação: 2019 Tipo de documento: Article