首页 / 院系成果 / 成果详情页

Randomized, Double-Blinded, Multicenter, Placebo-Controlled Trial of Shenfu Injection for Treatment of Patients with Chronic Heart Failure during the Acute Phase of Symptom Aggravation (Yang and Qi Deficiency Syndrome)  期刊论文  

  • 编号:
    fe96d699-6696-4ea2-b7f8-88e163385b6c
  • 作者:
    Wang, Xianliang#[1]Zhao, Zhiqiang[1];Mao, Jingyuan*[1]Du, Tinghai[2];Chen, Yuanping[3];Xu, Hao[4];Liu, Nan[5];Wang, Xiaolong(王肖龙)[6]Wu, Jianguang[7];Li, Rong[5];Xu, Yong[8];Zhao, Yingqiang[9];Wang, Lei[10];He, Jingsong[11];Zhang, Junhua[12];Zhai, Jingbo[12];Zhao, Guoyuan[1];Hou, Yazhu[1];Wang, Shuai[1];Liu, Chunxiang[12];
  • 语种:
    英文
  • 期刊:
    EVIDENCE-BASED COMPLEMENTARY AND ALTERNATIVE MEDICINE ISSN:1741-427X 2019 年 2019 卷
  • 收录:
  • 摘要:

    Background. Shenfu injection (SFI) has shown a remarkable therapeutic effect in patients with chronic heart failure (CHF) during the acute phase of symptom aggravation since it became commercially available in 1987. However, the therapeutic effect of SFI has not been validated in a standard clinical study. As a pilot clinical trial, this study aimed to evaluate the safety and efficacy of SFI for treatment of CHF patients during the acute phase. Methods. A total of 160 patients experiencing acute phase CHF were enrolled in this study and randomly assigned to receive the placebo (placebo group, 150 ml glucose (GS)) or SFI (SFI group, 50 ml SFI + 100 ml GS) in addition to their standard medications for CHF treatment. The treatment lasted for 7 +/- 1 days, and the follow-up continued for 28 +/- 3 days after treatment. The primary endpoints were New York Heart Association (NYHA) classification and Traditional Chinese Medicine (TCM) syndrome scores. Results. After 7 +/- 1 days of treatment, the efficacy of SFI according to improvements in NYHA and TCM syndrome scores in the SFI group (78.38% and 89.19%, respectively) was significantly higher than that in the placebo group (61.43% and 60.00%, respectively; P<0.05). The SFI group had a longer increase in amplitude than the placebo group (113.00 m versus 82.99 m, P<0.05). The incidence of adverse events and other safety indices showed no significant differences between the two groups. Conclusion. SFI combined with conventional therapy for treatment of CHF during acute symptom aggravation ameliorated the cardiac dysfunction and clinical symptoms and improved the patients' quality of life without any significant AEs compared with the conventional therapy alone.

  • 推荐引用方式
    GB/T 7714:
    Wang Xianliang,Zhao Zhiqiang,Mao Jingyuan, et al. Randomized, Double-Blinded, Multicenter, Placebo-Controlled Trial of Shenfu Injection for Treatment of Patients with Chronic Heart Failure during the Acute Phase of Symptom Aggravation (Yang and Qi Deficiency Syndrome) [J].EVIDENCE-BASED COMPLEMENTARY AND ALTERNATIVE MEDICINE,2019,2019.
  • APA:
    Wang Xianliang,Zhao Zhiqiang,Mao Jingyuan,Du Tinghai,&Liu Chunxiang.(2019).Randomized, Double-Blinded, Multicenter, Placebo-Controlled Trial of Shenfu Injection for Treatment of Patients with Chronic Heart Failure during the Acute Phase of Symptom Aggravation (Yang and Qi Deficiency Syndrome) .EVIDENCE-BASED COMPLEMENTARY AND ALTERNATIVE MEDICINE,2019.
  • MLA:
    Wang Xianliang, et al. "Randomized, Double-Blinded, Multicenter, Placebo-Controlled Trial of Shenfu Injection for Treatment of Patients with Chronic Heart Failure during the Acute Phase of Symptom Aggravation (Yang and Qi Deficiency Syndrome)" .EVIDENCE-BASED COMPLEMENTARY AND ALTERNATIVE MEDICINE 2019(2019).
  • 条目包含文件:
    文件类型:PDF,文件大小:
    正在加载全文
浏览次数:137 下载次数:0
浏览次数:137
下载次数:0
打印次数:0
浏览器支持: Google Chrome   火狐   360浏览器极速模式(8.0+极速模式) 
返回顶部