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A multi-center randomized controlled clinical trial on patients with coronary heart disease with qi stagnation and blood stasis syndrome

Clinical trial on patients with coronary heart disease with qi stagnation and blood stasis syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-15006989
Enrollment
Unknown
Registered
2015-08-25
Start date
2015-10-08
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

Huoxue Group:Taohongsiwu granules
Liqi Group:Xuefuzhuyu without Taohongsiwu granules
Liqi Huoxue Group:Xuefuzhuyu granules

Sponsors

Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Meeting the diagnosis of coronary heart disease; 2. Patients with qi stagnation and blood stasis syndrome by TCM as follws: Main symptoms: Chest pain and chest tightness. Accompanying symptoms: fullness in chest and hypochondrium, palpitations, dark purple tongue and uneven pulse; 3. Age: 40-60 years old; 4. I-II Cardiac function (NYHA cardiac functional grading); 5. Subjects was informed and signed informed consent voluntarily.

Exclusion criteria

Exclusion criteria: 1. Renal insufficiency: serum creatinine>2.5mg/dl (>220umo/l) in male or >2.0mg/dl (>175umo/l) in famale; 2. Significant liver disease, or ALT, AST three times higher than the upper limit of normal reference value; 3. Systolic blood pressure>160mmHg or diastolic blood pressure>100mmHg after controlling (patients need to sit for at least 5 minutes before the measurement of blood pressure); 4. Random blood glucose>=13.7mmol/L in patients with diabetes or glycated hemoglobin>=9.5%; 5. Pregnancy or women preparing for pregnant, breastfeeding women and the persons allergic to the known ingredients of the study drugs; 6. Patients combined with acute cerebrovascular disease; 7. Patients with malignant or life expectancy less than 3 years; 8. Patients with severe disease of hematopoietic system; 9. Severe mental illness; 10. Pateints who has participated or are participating in other clinical trials in three months.

Design outcomes

Primary

MeasureTime frame
TCM symptom classification quantitative score;Depression Scale;End Point;Resting ECG;Gasotransmitters;ATP in serum;Circulating non-coding RNA;Vasoactive peptide;Microvascular function;

Secondary

MeasureTime frame
Echocardiography;BNP;RAAS;CRP;Homocysteine;CD62P;Thromboelastography;Routine blood test;Routine urine test;Routine stool test;Liver and kidney function;Coagulation function;

Countries

China

Contacts

Public ContactXiuhua Liu
liuxiuhua98@163.com+86 010-66939763

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 14, 2026