FOLLOWUS
1. Beijing University of Chinese Medicine,Beijing,China
2. Senior Cardre Department, Xiyuan Hospital of China Academy of Chinese Medical Sciences,Beijing,China
3. Beijing Hospital of Traditional Chinese Medicine,Beijing,China
4. Affiliated Hospital of Liaoning University of Traditional Chinese Medicine,Shenyang,China
5. Affiliated Hospital of Shaanxi Chinese Medical College,Shaanxi Province,Xianyang,China
6. Second Affiliated Hospital of Tianjin University of Traditional Chinese Medicine,Tianjin,China
7. Affiliated Hospital of Chengdu University of Traditional Chinese Medicine,Chengdu,China
8. Hubei Provincial Hospital of Traditional Chinese Medicine,Wuhan,China
纸质出版日期:2015,
网络出版日期:2015-1-3,
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Zhang, Zf., Xu, Fq., Liu, Hx. et al. A multicenter, randomized, double-blind clinical study on Wufuxinnaoqing Soft Capsule (五福心脑清胶囊) in treatment of chronic stable angina patients with blood stasis syndrome., Chin. J. Integr. Med. 21, 571–578 (2015). https://doi.org/10.1007/s11655-014-1953-9
Zhi-fang Zhang, Feng-qin Xu, Hong-xu Liu, et al. A multicenter, randomized, double-blind clinical study on Wufuxinnaoqing Soft Capsule (五福心脑清胶囊) in treatment of chronic stable angina patients with blood stasis syndrome[J]. Chinese Journal of Integrative Medicine, 2015,21(8):571-578.
Zhang, Zf., Xu, Fq., Liu, Hx. et al. A multicenter, randomized, double-blind clinical study on Wufuxinnaoqing Soft Capsule (五福心脑清胶囊) in treatment of chronic stable angina patients with blood stasis syndrome., Chin. J. Integr. Med. 21, 571–578 (2015). https://doi.org/10.1007/s11655-014-1953-9 DOI:
Zhi-fang Zhang, Feng-qin Xu, Hong-xu Liu, et al. A multicenter, randomized, double-blind clinical study on Wufuxinnaoqing Soft Capsule (五福心脑清胶囊) in treatment of chronic stable angina patients with blood stasis syndrome[J]. Chinese Journal of Integrative Medicine, 2015,21(8):571-578. DOI: 10.1007/s11655-014-1953-9.
To confirm the efficacy and safety of Wufuxinnaoqing Soft Capsule (五福心脑清胶囊
WSC) in the treatment of chronic stable angina (blood stasis syndrome). A multicenter
randomized
double-blind
placebo-controlled trial with superiority test was designed. A total of 240 patients with chronic stable angina (blood stasis syndrome) from multiple centers were randomly and equally assigned to the treatment group and the control group. Based on standard treatment of Western medicine
the treatment group was given WSC
while the control group was given WSC mimetic
both for 12 weeks. Observed indicators included the efficacy in angina
the efficacy in Chinese medicine syndrome
the withdrawal or reduce rate of nitroglycerin and routine safety indices. After 12-week treatment
the significant effective rate and total effective rate of the treatment group were significantly better than those of the control group (23.5% vs. 9.2%
64.7% vs. 30.8%)
respectively
with statistically significant difference (P<0.01). After 12-week treatment
the decreased points and the decreased rate of angina symptom score in the treatment group were better than in the control group (5.1±4.2 points vs. 2.8±3.5 points
44.9%±37.2% vs. 25.4%±30.7%) respectively
with significant difference (P<0.01). After 12-week treatment
the significant effective rate and total effective rate of the treatment group were better than the control group (respectively
30.3% vs. 15.0%
67.2% vs. 45.0%
P<0.01). After 8- or 12-week treatment
the decreased points and the decreased rate of Chinese medicine syndrome score in the treatment group were better than the control group (P<0.05 orP<0.01). After 12-week treatment
nitroglycerin withdrawal rate and the withdrawal or reduce rate in treatment group were better than the control group (P<0.01). On safety evaluation
the incidence of adverse events (7.563% vs. 7.500%) and the incidence of cardiovascular events (0.840% vs. 0.000%) in the treatment group were similar with the control group
and the difference was not statistically significant (P>0.05). In treatment of chronic stable angina (blood stasis syndrome)
WSC can reduce angina attacks and consumption of nitroglycerin
decrease angina severity degree
effectively relieve the blood stasis syndromes
such as chest pain
chest tightness
palpitations
dark purple tongue and other symptoms. Besides
adverse events and cardiovascular adverse events in the treatment group and the control group showed no difference. All shows that the drug is safe and effective. [This study was registered in Chinese Clinical Trial Registry (ChiCTR)
with registration number: ChiCTR-TRC-14005158.]
To confirm the efficacy and safety of Wufuxinnaoqing Soft Capsule (五福心脑清胶囊
WSC) in the treatment of chronic stable angina (blood stasis syndrome). A multicenter
randomized
double-blind
placebo-controlled trial with superiority test was designed. A total of 240 patients with chronic stable angina (blood stasis syndrome) from multiple centers were randomly and equally assigned to the treatment group and the control group. Based on standard treatment of Western medicine
the treatment group was given WSC
while the control group was given WSC mimetic
both for 12 weeks. Observed indicators included the efficacy in angina
the efficacy in Chinese medicine syndrome
the withdrawal or reduce rate of nitroglycerin and routine safety indices. After 12-week treatment
the significant effective rate and total effective rate of the treatment group were significantly better than those of the control group (23.5% vs. 9.2%
64.7% vs. 30.8%)
respectively
with statistically significant difference (P<0.01). After 12-week treatment
the decreased points and the decreased rate of angina symptom score in the treatment group were better than in the control group (5.1±4.2 points vs. 2.8±3.5 points
44.9%±37.2% vs. 25.4%±30.7%) respectively
with significant difference (P<0.01). After 12-week treatment
the significant effective rate and total effective rate of the treatment group were better than the control group (respectively
30.3% vs. 15.0%
67.2% vs. 45.0%
P<0.01). After 8- or 12-week treatment
the decreased points and the decreased rate of Chinese medicine syndrome score in the treatment group were better than the control group (P<0.05 orP<0.01). After 12-week treatment
nitroglycerin withdrawal rate and the withdrawal or reduce rate in treatment group were better than the control group (P<0.01). On safety evaluation
the incidence of adverse events (7.563% vs. 7.500%) and the incidence of cardiovascular events (0.840% vs. 0.000%) in the treatment group were similar with the control group
and the difference was not statistically significant (P>0.05). In treatment of chronic stable angina (blood stasis syndrome)
WSC can reduce angina attacks and consumption of nitroglycerin
decrease angina severity degree
effectively relieve the blood stasis syndromes
such as chest pain
chest tightness
palpitations
dark purple tongue and other symptoms. Besides
adverse events and cardiovascular adverse events in the treatment group and the control group showed no difference. All shows that the drug is safe and effective. [This study was registered in Chinese Clinical Trial Registry (ChiCTR)
with registration number: ChiCTR-TRC-14005158.]
Wufuxinnaoqing Soft Capsulechronic stable anginaBlood Stasis SyndromeChinese medicine therapy
Wufuxinnaoqing Soft Capsulechronic stable anginaBlood Stasis SyndromeChinese medicine therapy
Xiong YL, Wang YL, Wu YH, Sun JH, Wu ZL, He R, et al. Pharmacodynamic studies of Wufuxinnaokang. Chin J Inform Tradit Chin Med (Chin) 2004;5:393-395.
Wu YH, Wang YL, Xiong YL, Sun JH, Zhou ZM, Wang QL, et al. Study on therapeutic effect of Wufuxinnaoqing in rats with focal cerebral infarction. China J Exp Tradit Med Formulae (Chin) 2005;3:35-36.
Wu YH, Wang YL, Xiong YL, Sun JH, Zhou ZM, Wang QL, et al. Study on protective effect of Wufuxinnaoqing on the cardiovascular system in rats. China J Chin Mater Med (Chin) 2005;11:876-877.
Ma H, Shen LH, Gao RL, Qi WH, Huo Y. Guideline of diagnosis and treatment in chronic stable angina. Chin J Cardiol (Chin) 2007;35:195-206.
Raymond JG, Jonathan A, Kanu C, Jennifer D, Prakash CD, John SD, et al. ACC/AHA. 2002 guideline update for the management of patients with chronic stable angina. J Am Coll Cardiol 2003;41:159-168.
China Food and Drug Administration. Guidelines of clinical research technology in treatment of angina pectoris with Chinese medicine or natural medicine. 2011. Available at http://www.doc88.com/p-203832734008.html
Campeau L. Letter: Grading of angina pectoris. Circulation 1976;54:522-523.
zheng YY, Ren DQ, Cao WZ, Tao XS, Zhang J, Xie SC, et al. New drugs of Chinese medicine dinical research guiolelines (Trial). Beijing: China Medical Science Press; 2002:68-73.
Xu RY, Tong SH. Studies on chemical constituents and pharmacological effects of safflower. J China Pharm (Chin) 2010;20:86-87.
Jia JJ, Miao MS. Modern research and new applications of safflower. China J Chin Med (Chin) 2013;11:1682-1685.
Wei CR, Wu GQ. Research advance in pharmacological effect of borneol and the underlying mechanism. Int J Pathol Clin Med (Chin) 2010;4:447-451.
Sun XY. Pharmacology research and new applications of vitamin E. Chin Med Modern Distance Education China (Chin) 2010;9:230-231.
Zhang W, Yao J, Pham V, Whitney T, Froese D, Friesen A, et al. Pyridoxine as a template for the design of antiplatelet agents. Bioorg Med Chem Lett 2004;18:4747-4750.
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