Status:
UNKNOWN
Efficacy and Safety of Xueshuanxinmaining Tablet for the Treatment of Stable Angina Pectoris
Lead Sponsor:
Guang'anmen Hospital of China Academy of Chinese Medical Sciences
Conditions:
Coronary Heart Disease
Stable Angina
Eligibility:
All Genders
30-75 years
Phase:
PHASE4
Brief Summary
This study is a randomized, double-blind, placebo-controlled, parallel clinical trial in Chinese population with stable angina pectoris. The purpose is to determine the efficacy and safety of Xueshuan...
Detailed Description
Xueshuanxinmaining tablet is a Chinese patent medicine composed of Ligusticum chuanxiong, Salvia miltiorrhiza, borneol and Toad puff, etc. It has been widely used in cardiovascular diseases in China. ...
Eligibility Criteria
Inclusion
- Participants are aged between 40 and 75 years.
- Meet the diagnostic criteria of stable angina pectoris.
- Meet Chinese medicine syndrome differentiation of Qi-yin deficiency and blood stasis syndrome.
- Voluntarily participate and sign informed consent.
Exclusion
- Patients were diagnosed as acute myocardial infarction, unstable angina, stable exertion angina and other heart diseases.
- Patients with poor control of hypertension and diabetes, severe cardiopulmonary insufficiency, severe arrhythmia (rapid atrial fibrillation, atrial flutter, paroxysmal ventricular tachycardia, etc.), with a history of heart pacemaker or cerebrovascular disease within one year.
- Any of the following disease history or evidence was found in the screening period: severe cardiovascular or cerebrovascular diseases; active, recurrent peptic ulcer or other bleeding risk diseases; other serious diseases of digestive system; combined with malignant tumor, blood system disease, serious or progressive diseases of the other system; combined with mental diseases.
- Before screening, any laboratory inspection index meets the following standards: The results showed that Glutamic aspartate transaminase (AST) or alanine aminotransferase (ALT) were more than 1.5 times of the upper limit of normal value and serum creatinine (Cr) was more than 1.2 times of the upper limit of normal value.
- With a history of alcohol and drug abuse.
- Pregnant or lactating women.
- Patients who have participated in clinical trials of other drugs within 3 months before enrollment.
Key Trial Info
Start Date :
December 1 2020
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
October 1 2021
Estimated Enrollment :
120 Patients enrolled
Trial Details
Trial ID
NCT04270279
Start Date
December 1 2020
End Date
October 1 2021
Last Update
November 13 2020
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