Skip to content

Clicinal Study of Qing-xin-jie-yu Decoction on Elevated Serum Levels of Inflammatory Markers in Patients with Stable Coronary Heart Disease

A Random Double-Blinded Placebo-Controlled Trial for Qingxin Jieyu Decoction on Reducing Inflammatory Markers in Patients with Stable Coronary Heart Disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900020484
Enrollment
Unknown
Registered
2019-01-02
Start date
2015-10-01
Completion date
Unknown
Last updated
2019-01-14

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

Conditions

coronary heart disease

Interventions

group1: conventional therapy combine with Qing-xin -Jie-yu Decoction
group2:conventional therapy combine with placebo

Sponsors

Xiyuan Hospital Affiliated to the China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Those with a definite history of MI, or coronary stenosis (> 50%) confirmed by coronary angiography or spiral CT, or stable condition (> 1 month) after treatment of acute coronary syndrome (ACS) (PCI or drug intervention); 2. Aged 18 to 75 years; 3. High sensitivity C-reactive protein was found between 3 and 10 mg/L; 4. Signed informed consent.

Exclusion criteria

Exclusion criteria: 1. having a history of AMI, UA Underwent PCI or CABG less than one months; 2. Having Other heart diseases, Severe cardiopulmonary dysfunction; 3. bad-controlled hypertension (systolic blood pressure >=160mmHg and diastolic blood pressure >=100mmHg); 4. Having Acute cerebrovascular disease; 5. Having other serious primary diseases of hepatic, renal and hematopoietic system, or psychosis; 6. malignancy arrhythmia (such as paroxysmal ventricular tachycardia) are relapsing repeatedly recently; 7. Woman in Pregnancy, Planned pregnancy or lactation period; 8. Underwent craniocerebral, thoracic and abdominal operation in the past four weeks and having bleeding tendency; 9. participated in other clinical trials in the past a month; 10. allergic constitution or a known allergy to the study medication.

Design outcomes

Primary

MeasureTime frame
high-sensitivity c-reactive protein;

Secondary

MeasureTime frame
sCD40L;MMP-9;IL-6;TNF-a;sVCAM-1;SDS;angina pectoris grade;BSS score;Electrocardiogram;hyperlipidemia;Seattle angina questionnaire;TCM syndrome;MCP-1;

Contacts

Public ContactXu Hao

Xiyuan Hospital Affiliated to the China Academy of Chinese Medical Sciences

xuhaotcm@hotmail.com+86 010-62835341

Outcome results

None listed

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