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Clinical Trial Summary

This study is a prospective, multicentre, randomized, open-label, blinded-endpoint clinical trial to evaluate the efficacy and safety of Yangxinshi tablets in the treatment of patients with chronic coronary syndrome (CCS).


Clinical Trial Description

This study plans to enrol 1200 CCS patients. A central randomized control group will be set up. The experimental and control groups will be populated at a 3:1 ratio. In addition to basic medication, the experimental group will be given Yangxinshi tablets (three tablets each time, three times a day); the control group will be given basic medication only. The treatment period is 24 weeks. The primary efficacy indicator is the 6-minute walking distance (6MWD). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06171061
Study type Interventional
Source Shandong First Medical University
Contact Yuan Haitao
Phone 0531-68776356
Email doctoryuanht@126.com
Status Recruiting
Phase Phase 4
Start date December 18, 2023
Completion date December 31, 2026

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