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Clinical investigation on the evolution law of phlegm and blood stasis syndrome in patients with coronary heart disease

Innovation Research Based on syndrome differentiation of phlegm and blood stasis syndrome differentiation of coronary heart disease

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-EOC-16009965
Enrollment
Unknown
Registered
2016-11-22
Start date
2016-12-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Coronary Heart Disease

Interventions

Metabolic Syndrome Group:Null
Stable stable Coronary Heart Disease:Null
Acute Coronary Syndrome/Percutaneous Coronary Intervention/ Coronary Artery Bypass Graft Group:Null
Heart Failure Based on Coronary Heart Disease Group:Null

Sponsors

China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) the patient who aged from 35 to 85 years; (2) the patient who had signed the informed consent form and voluntarily participated in the study.

Exclusion criteria

Exclusion criteria: (1) patients with infection, fever, trauma, burns, surgical history, or active tuberculosis or rheumatic diseases in the past 1 weeks; (2) patients with heart valve disease (a valve and more than the occurrence of moderate lesions) or primary cardiomyopathy; (3) patients with acute exacerbation of chronic obstructive pulmonary disease or chronic pulmonary heart disease or respiratory failure; (4) patients with known renal insufficiency, serum creatinine (Cr) male > 221umol/L, female > 177 umol/L; (5) patients with known liver dysfunction, alanine aminotransferase (ALT) > 3 times the normal value of the patients with cirrhosis; (6) patients with severe primary diseases such as hematopoietic system or malignant tumor; (7) organ transplant patients; (8) patients with severe mental disorders (perceived barriers, mental disorders); (9) pregnant women and lactating women; (10) the researchers think that there are not suitable to participate in the study of other circumstances

Design outcomes

Primary

MeasureTime frame
TCM Syndrome Evaluation Scale;

Countries

China

Contacts

Public ContactHu Jingqing

Institution of Basic Theory of Traditional Chinese Medicine, China Academy of Chinese Medical Sciences

gcp306@126.com+86 13911546633

Outcome results

None listed

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