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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03179514
Other study ID # GLXB-2017
Secondary ID
Status Not yet recruiting
Phase Phase 4
First received June 5, 2017
Last updated June 5, 2017
Start date July 2017
Est. completion date December 2019

Study information

Verified date June 2017
Source Guang'anmen Hospital of China Academy of Chinese Medical Sciences
Contact Panpan Tian
Phone +86 15652388175
Email 15652388175@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study evaluates the clinical efficacy of Gualou Xiebai Banxia Decoction compounded with Danshen Decoction in the treatment of unstable angina pectoris. All of the patients will be divided into 2 arms randomly. One of the arms will be treated by conventional western medicine, the other one will be treated by Gualou Xiebai Banxia Decoction compounded with Danshen Decoction at the base of conventional western medicine.


Description:

Gualou Xiebai Banxia Decoction compounded with Danshen Decoction has the effect of promoting blood circulation and resolving phlegm, so it will be used for patients taht belong to phlegm and blood stasis type.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 120
Est. completion date December 2019
Est. primary completion date October 2019
Accepts healthy volunteers No
Gender All
Age group 35 Years to 70 Years
Eligibility Inclusion Criteria:

- Participants diagnosed with coronary heart disease through coronary angiography or coronary CTA;

Patients have at least one of these symptoms:

1. The stability of the nature of angina pectoris changes, that is, frequent attacks of angina pectoris, serious degree and prolonged duration;

2. Angina pectoris during rest;

3. The recent occurrence of angina pectoris caused by mild physical activity in the last month.

Exclusion Criteria:

- Patients diagnosed with stable angina; Patients with acute myocardial infarction; Chest pain caused by congenital heart disease, valvular heart disease, severe neurosis or arrhythmia; The heart function grade is III or IV; Patients with acute cerebral infarction; Patients complicated with other serious primary diseases; Patients with acute infection in recent 2 weeks; Uncontrolled hypertension (the resting blood pressure >160/95mmHg within one week); Diabetics emerged with serious diabetic complications; Patients can't finish the questionnaire due to abnormal mental and nervous or mental disorders; Pregnant or lactating women.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Anti-Platelet Drugs
Including aspirin and clopidogrel, etc.
Lipid Regulating Drugs
Mainly including statins
Coronary Vasodilator
Mainly including nitrates
Gualou Xiebai Banxia Decoction & Danshen Decoction
Mainly including Fructus Trichosanthis, Rhizoma Pinelliae, Allium, Salvia Miltiorrhiza etc.

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Jun Li Guang'anmen Hospital of China Academy of Chinese Medical Sciences

References & Publications (4)

Liu W, Xiong X, Yang X, Chu F, Liu H. The Effect of Chinese Herbal Medicine Gualouxiebaibanxia Decoction for the Treatment of Angina Pectoris: A Systematic Review. Evid Based Complement Alternat Med. 2016;2016:8565907. Epub 2016 Sep 29. Review. — View Citation

Qiu Y, Xu H, Shi D. Traditional chinese herbal products for coronary heart disease: an overview of cochrane reviews. Evid Based Complement Alternat Med. 2012;2012:417387. doi: 10.1155/2012/417387. Epub 2012 Mar 28. — View Citation

Wang J, Yang X, Chu F, Chen J, He Q, Yao K, Teng F, Gao Y, Xing Y, Wu A, Xing Y. The effects of xuefu zhuyu and shengmai on the evolution of syndromes and inflammatory markers in patients with unstable angina pectoris after percutaneous coronary intervent — View Citation

Wang J, Yu G. A Systems Biology Approach to Characterize Biomarkers for Blood Stasis Syndrome of Unstable Angina Patients by Integrating MicroRNA and Messenger RNA Expression Profiling. Evid Based Complement Alternat Med. 2013;2013:510208. doi: 10.1155/20 — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Mortality Death caused by cardiovascular disease Six months after drug intervention
Secondary Myocardial enzymes The unit is mmol/L At baseline and 4 weeks after drug intervention
Secondary lood lipid The unit is mmol/L. Blood lipid The unit is mmol/L. At baseline and 4 weeks after drug intervention
Secondary Treadmill exercise test The result will be positive or negative. At baseline and 4 weeks after drug intervention
Secondary The incidence of myocardial infarction or heart failure Six months after drug intervention] Inclusion Criteria:
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