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Clinical Trial Summary

This study adopted a randomized, double-blind, placebo-controlled, multicenter clinical design and compared the effects of Yangxinshi tablet and placebo on exercise tolerance in patients with chronic coronary syndrome (CCS).


Clinical Trial Description

The aim of the research is to find out if the addition of Yangxinshi tablets on the basis of conventional treatment can improve exercise tolerance of patients with chronic coronary syndrome (CCS), improve quality of life and mental health. A total of 120 qualified CCS patients were randomly divided into two groups. In addition to conventional treatment, the experimental group was given Yangxinshi tablets (3 tablets/time and 3 times/day), and the control group was given Yangxinshi tablet simulants (3 tablets/time and 3 times/day). The treatment period was 24 weeks. The primary endpoints were metabolic equivalents (METs), and peak oxygen uptake measured by cardiopulmonary exercise testing after 24 weeks of treatment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05978089
Study type Interventional
Source Dongzhimen Hospital, Beijing
Contact Wang Xian
Phone 010-84013276
Email wx650515@163.com
Status Recruiting
Phase Phase 4
Start date November 8, 2023
Completion date December 2025

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