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Clinical study of Chinese herbal compound Qidan Xiaoke Granules in patients after coronary revascularization

Clinical study of Chinese herbal compound Qidan Xiaoke Granules in patients after coronary revascularisation surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026001326
Enrollment
Unknown
Registered
2026-05-26
Start date
2026-07-01
Completion date
Unknown
Last updated
2026-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Following coronary revascularisation surgery

Interventions

Experimental Group:Standardized Western medical treatment + Qidan Xiao Ke Granules
Control Group:Standardized Western medical treatment + Qidanshaoke granules placebo

Sponsors

The Third Affiliated Hospital of Zhejiang University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18-80 years old; 2. no gender limitation; 3. Meets the diagnostic criteria for coronary heart disease; 4. Accepts effective PCI procedure; 5. Voluntarily participates and signs a written informed consent form.

Exclusion criteria

Exclusion criteria: 1. Severe hepatic and/or renal insufficiency 2. Severe electrolyte disorders 3. Severe hematological diseases or malignant tumors 4. Pregnant or breastfeeding women 5. Patients with mental illness 6. Cognitive impairment (e.g., dementia, post-stroke cognitive impairment) leading to inability to communicate normally 7. Planning to undergo another revascularization surgery in the near future 8. Other severe cardiovascular diseases (e.g., uncontrolled hypertension, angina pectoris, rapid arrhythmias, high-degree or complete atrioventricular block without a pacemaker implanted, acute severe aortic stenosis, decompensated heart failure (NYHA Class IV), deep vein thrombosis, obstructive hypertrophic cardiomyopathy, acute pericarditis or myocarditis, acute endocarditis, acute aortic dissection, etc.) 9. Acute pulmonary embolism and chronic lung diseases with dyspnea symptoms (occurring at rest or with minimal exertion) 10. Explicit exclusion criteria (bleeding history within 1 month, active bleeding, bleeding tendency, currently using anticoagulants) 11. Participants in other interventional clinical trials within the past month 12. Allergy to known components of the investigational drug (Qidan Xiaohe Granules) 13. Other conditions deemed unsuitable for participation in the trial by the investigator

Design outcomes

Primary

MeasureTime frame
The incidence rate of major cardiovascular adverse events;

Secondary

MeasureTime frame
TCM Syndrome Score;Echocardiogram;Dynamic Electrocardiogram;Minnesota Quality of Life Scale;Cardiac enzymes;blood lipids;Blood Glucose;

Countries

China

Contacts

Public ContactLiu Qiang

The Third Affiliated Hospital of Zhejiang University of Chinese Medicine

19981011@zcmu.edu.cn13588121905

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Jun 11, 2026