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Biological basis of cell interaction therapy for coronary microcirculation disorders and intervention mechanism of Huoxue Wentong formula - a randomized controlled clinical study on the intervention of Huoxue Wentong formula in patients with coronary microcirculation disorders

Biological basis of cell interaction therapy for coronary microcirculation disorders and intervention mechanism of Huoxue Wentong formula - a randomized controlled clinical study on the intervention of Huoxue Wentong formula in patients with coronary microcirculation disorders

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025000367
Enrollment
Unknown
Registered
2025-02-19
Start date
2024-09-02
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Coronary microcirculation disorder

Interventions

Test group:Huoxue Wentong Formula Combined with Basic Treatment
Control group:Blood activating and warming formula placebo plus basic treatment

Sponsors

Guang'anmen Hospital Chinese Academy of Chinese Medicine Science
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 79 Years

Inclusion criteria

Inclusion criteria: 1) Meets the Western diagnostic criteria for primary stable microvascular angina; 2) Men or women aged 18-79 years old; 3) Traditional Chinese medicine syndrome differentiation conforms to the Yang deficiency and blood stasis syndrome; 4) Not taking traditional Chinese medicine within one week; 5) Sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1) After PCI coronary artery bypass grafting and old myocardial infarction; 2) Heart muscle bridge; 3) The electrocardiogram shows ST elevation changes or coronary angiography shows coronary spasm; 4) Severe mitral valve disease dilated or hypertrophic cardiomyopathy myocarditis congenital heart disease; 5) Grade II or above atrioventricular block or severe arrhythmia; 6) Has non ischemic chest pain; 7) Cardiac function level III-IV (NYHA); 8) Left ventricular ejection fraction<50%; 9) Unable to simultaneously complete coronary angiography/coronary CTA and transthoracic Doppler echocardiography; 10) Having severe chronic obstructive pulmonary disease (such as asthma bronchiectasis emphysema pulmonary fibrosis etc.); 11) Suffering from acute pulmonary embolism or acute cerebral infarction; 12) Systemic hypotension (systolic blood pressure<90mmHg); 13) Has immune system diseases such as vasculitis; 14) Having mental illnesses; 15) Performing major surgical procedures in the past 3 months; 16) Pregnant pregnant or lactating women; 17) Decreased cognitive ability that prevents them from taking medication or completing laboratory tests as required by the experiment; Cancer patients or those with an expected lifespan of less than 4 years; 18) Patients with abnormal liver function and renal insufficiency (blood creatinine and urea nitrogen exceeding 1.2 times the normal range); 19) Individuals who are allergic to relevant drugs and have an allergic constitution.

Design outcomes

Primary

MeasureTime frame
Single-Photon Emission Computed TomographySPECT;CFR;

Secondary

MeasureTime frame
SAQ;Cardiopulmonary Exercise TestingCPX;Scoring of Traditional Chinese Medicine Four Diagnostic Information;

Countries

China

Contacts

Public ContactXiong Xingjiang

Guang'anmen Hospital Chinese Academy of Chinese Medicine Science

5administration@163.com15801463736

Outcome results

None listed

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