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An evidence-based evaluation of blood-activating and detoxifying intervention in unstable angina and research on its anti-inflammatory mechanisms

An evidence-based evaluation of blood-activating and detoxifying intervention in unstable angina and research on its anti-inflammatory mechanisms

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025000276
Enrollment
Unknown
Registered
2025-02-15
Start date
2025-02-20
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

Unstable angina pectoris

Interventions

Trial Group:Placebo groupconventional therapycombine with Qing-Xin-Jie-Yu Granule
Placebo group:conventional therapycombine with paceDo

Sponsors

Xiyuan Hospital China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1)35 years = age =75 years 2)The diagnostic criteria of unstable angina were met 3)The syndrome differentiation of TCM belongs to the syndrome of stasis and toxin 4)hs-CRP=2mg/L 5)Volunteer and sign the informed consent form

Exclusion criteria

Exclusion criteria: Anyone who meets any of the following conditions will be excluded: 1)Individuals with heart diseases caused by conditions other than coronary artery disease such as primary cardiomyopathy or infective endocarditis. 2)Individuals who have had infections fever trauma burns or surgeries within the past month. 3)Individuals with a tendency to bleed or low platelet count. 4)Individuals currently using antibiotics or traditional Chinese medicine for clearing heat and detoxification. 5)Individuals with severe heart failure and left ventricular ejection fraction (LVEF) < 50%. 6)Individuals with malignant arrhythmias (paroxysmal ventricular tachycardia) who have had frequent recent episodes. 7)Individuals with malignant tumors active autoimmune diseases or tuberculosis. 8)Pregnant women women planning pregnancy or breastfeeding women. 9)Individuals who have participated in other clinical trials within the past month or individuals with expected poor compliance or individuals allergic to the components of the trial medication.

Design outcomes

Primary

MeasureTime frame
hs-CRP;

Secondary

MeasureTime frame
Levels of other inflammatory factors;Cardiac function parameters;brain natriuretic peptide;Seattle Angina Questionnaire;Adverse cardiovascular events;

Countries

China

Contacts

Public ContactHao Xu

Xiyuan Hospital China Academy of Chinese Medical Sciences

xuhaotcm@hotmail.com18601081161

Outcome results

None listed

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