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Clinical Study on TCM Syndrome law and whole process TCM management of coronary artery disease

Clinical Study on TCM Syndrome law and whole process TCM management of coronary artery disease

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200059404
Enrollment
Unknown
Registered
2022-04-29
Start date
2022-07-30
Completion date
Unknown
Last updated
2024-09-30

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

Conditions

coronary heart disease

Interventions

Western conventional treatment + Chinese medicine treatment group (Part 2):None
Western conventional treatment group (part two):None
Coronary artery disease observation group (part one):None
Coronary heart disease chest pain pre hospital registration observation group:None

Sponsors

Wangjing hospital, China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Part one: 1. Respondents aged 30-70 years; 2. Meet the diagnostic criteria for each population; 3. Sign the Informed Consent Form and voluntarily participating in this study. Part two: 1. Age range from 30 to 70 years old, male or female not limited; 2. Meet the diagnostic criteria for stable angina pectoris; 3. Meet the diagnostic criteria of traditional Chinese medicine for chest obstruction, qi deficiency, and blood stasis type; 4. Sign the "Informed Consent" and voluntarily participate in this study.

Exclusion criteria

Exclusion criteria: Part one: 1. Patients with mental illness; 2. Individuals with severe liver and kidney dysfunction; 3. Participants in other studies; 4. Unable to cooperate with researchers; 5. Incomplete information affects the judgement. Part two: 1. History of myocardial infarction or unstable angina within 3 months, or coronary revascularization; 2. Combination of other cardiac diseases, neurosis, menopausal syndrome, hyperthyroidism, cervical rheumatism and other diseases that may cause chest pain; 3. Active liver disease, or with persistent elevation of serum transaminases of unknown cause, or upper limit of normal reference value of ALT; 4. Severe abnormal renal function; 5. Serious primary diseases such as combined respiratory, haematological or malignant neoplasm; 6. Pregnant or lactating women or women of childbearing age with childbearing requirements; 7. Patients with psychiatric disorders, or cognitive impairment; 8. Those with expected poor compliance and unable to follow up regularly; 9. Other conditions deemed by the investigator to exist that make participation in the study inappropriate.

Design outcomes

Primary

MeasureTime frame
Seattle angina questionnaire scores;

Secondary

MeasureTime frame
Incidence of cardiovascular events;Changes in TCM evidence scores;Anti-ischaemic drug applications;Haemodynamic indicators;Blood lipid indicators;

Countries

China

Contacts

Public ContactChenhao Zhang

Wangjing Hospital, China Academy of Chinese Medical Sciences

zhangch500@126.com+86 13671393316

Outcome results

None listed

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