Overview

Effect of Yangxinshi Tablet on Exercise Tolerance in Patients With Chronic Coronary Syndrome(MET STUDY)

Status:
Recruiting
Trial end date:
2025-12-01
Target enrollment:
0
Participant gender:
All
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).
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Dongzhimen Hospital, Beijing
Criteria
Inclusion Criteria:

All the following criteria must be met to participate in the study:

1. Meet the diagnostic criteria for CCS in Western medicine; stable coronary heart
disease (CHD) with a degree of coronary stenosis ≥50% by angiography or computed
tomography angiography (CTA) (including patients with more than 1 year of
revascularization)

2. Meet the TCM standard of Qi deficiency and blood stasis syndrome

3. MET < 5 measured by cardiopulmonary exercise test (treadmill)

4. Age between 18 and 75 years (including both age limits), with no limitation on sex

5. Understanding and voluntarily signing the written informed consent

Exclusion Criteria:

All the following criteria must not be met to participate in the study:

1. Individuals with lower extremity dysfunction, intermittent claudication or severe leg
pain who cannot participate in cardiopulmonary exercise tests

2. Individuals with acute coronary syndrome within 1 month after percutaneous coronary
intervention (PCI) or within 3 months after coronary artery bypass grafting (CABG)

3. Individuals with serious primary diseases related to the liver, kidney, and
hematopoietic system, acute infectious diseases, and mental illness and individuals
with other diseases who are not suitable for cardiopulmonary exercise tests

4. Individuals with a revascularization plan within a month

5. Individuals with left main stenosis ≥50% or proximal left anterior descending (LAD)
diameter stenosis ≥90% without PCI or CABG

6. Individuals with absolute and relative contraindications to cardiopulmonary exercise
testing (please see Appendix 11 for details)

7. Individuals with New York Heart Association (NYHA) cardiac function class III and IV

8. Individuals with acute cerebrovascular disease

9. Individuals with uncontrolled hypertension: systolic blood pressure ≥ 160 mmHg and
diastolic blood pressure ≥ 100 mmHg

10. Individuals found to be in a state of severe anxiety and depression as determined
using the GAD-7 and PHQ-9

11. Individuals with allergies or abnormal drug reactions to the test drugs

12. Women of childbearing age who are pregnant or breastfeeding, plan to get pregnant
within six months, have a positive pregnancy test, and cannot take effective
contraceptive measures during the study period

13. Individuals who have regularly taken YTs, Chinese herbal decoctions or proprietary
Chinese medicines with similar curative effects within the past 7 days (please refer
to Appendix 12 for the names of proprietary Chinese medicines)

14. Individuals who have participated in other clinical trials within the past 3 months

15. Individuals unsuitable for the clinical trials, as determined by the researchers