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Clinical efficacy and safety study of Qiyi Yiqi Decoction in treating unstable angina pectoris

Clinical efficacy and safety study of Qiyi Yiqi Decoction in treating unstable angina pectoris

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025001501
Enrollment
Unknown
Registered
2025-07-28
Start date
2025-07-30
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Unstable angina

Interventions

Experimental group:Standardized Western medicine treatment + Qi Dan Yi Qi Decoction (Standard Dosage)
control group:Standard Western medical treatment combined with Qiyi Yiqi Decoction (low dose)

Sponsors

Beijing Hospital of Traditional Chinese Medicine Affiliated to Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1)Age between 35 and 75 gender (2) Meet the diagnostic criteria for UA and meet one of the following three conditions: 1) Coronary angiography or coronary CT angiography confirms coronary heart disease; 2) Previous coronary revascularization treatment; 3) History of old myocardial infarction; (3) CCS angina classification is grade I-III; (4) Traditional Chinese Medicine diagnosis of Qi deficiency and blood stasis syndrome; (5) Signed informed consent form.

Exclusion criteria

Exclusion criteria: Patients who are pregnant or breastfeeding; those allergic to the trial drug components; those with severe heart failure (left ventricular ejection fraction < 30%) or serious arrhythmias (such as rapid atrial fibrillation ventricular fibrillation or ventricular tachycardia) or other heart diseases (valvular heart disease dilated cardiomyopathy restrictive cardiomyopathy cor pulmonale congenital heart disease etc.); those with severe infections chronic obstructive diseases respiratory failure or pulmonary heart disease; those with severe primary liver kidney or blood system diseases malignant tumors or severe mental illnesses or uncontrollable systemic diseases; those with severe metabolic disorders (such as hyperthyroidism diabetic ketoacidosis); those planning coronary artery revascularization within 30 days; or those currently using traditional Chinese medicines similar in composition or function to the study medication.

Design outcomes

Primary

MeasureTime frame
TyG index;Seattle Angina QuestionnaireSAQ;

Secondary

MeasureTime frame
Creatine Kinase-Myocardial Band;Fasting blood glucose;Total Cholesterol;Low Density Lipoprotein-Cholesterol;Optimal antiplatelet Therapy for Chinese patients with Coronary Artery Disease;Triglycerides;Hospital Anxiety and Depression Scale;High Density Lipoprotein-Cholesterol;Prediction of Bleeding Risk in Dual Antiplatelet Therapy;Creatine Kinase;Traditional Chinese Medicine syndrome scoring;

Countries

China

Contacts

Public ContactQiu Shenglei

Beijing TCM Hospital Affiliated with Capital Medical University

choushenglei@bjzhongyi.com13426241268

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026