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A Randomized Controlled Trial for the Effect of Yiqi Huoxue Decoction on Exercise Tolerance in Patients with Chronic Stable Coronary Heart Disease

A Randomized Controlled Trial for the Effect of Yiqi Huoxue Decoction on Exercise Tolerance in Patients with Chronic Stable Coronary Heart Disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900021608
Enrollment
Unknown
Registered
2019-03-01
Start date
2019-03-01
Completion date
Unknown
Last updated
2019-03-04

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

Conditions

Chronic Stable Coronary Disease

Interventions

control group :Trimetazidine

Sponsors

Dongfang Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Outpatient patients who meet the diagnostic criteria for chronic stable coronary heart disease: (1) Has a history of myocardial infarction, treated by or without revascularization (percutaneous coronary intervention or coronary artery bypass grafting); (2) Coronary angiography or coronary CT showed that the diameter of at least one main branch of the coronary artery is narrowed by more than 50%, and was treated with or without revascularization; 2. The type of TCM syndrome is Qi deficiency and blood stasis. 3. Patients aged 35-75 years; 4. Patients who volunteer to participate in the study and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. History of myocardial infarction or unstable angina pectoris, or coronary revascularization (percutaneous coronary intervention or coronary artery bypass grafting) has occurred within the past 60 days; 2. Patients with one of the following diseases: (1) Hypertension patients who still have high blood pressure after antihypertensive treatment (systolic blood pressure =180 mmHg, diastolic blood pressure =100 mmHg); (2) Severe arrhythmia (atrial fibrillation with rapid ventricular response, atrial flutter, paroxysmal attack); (3) Pulmonary heart disease, rheumatic heart disease, myocarditis, cardiomyopathy, aortic dissection, pulmonary embolism; 3. hyperthyroidism, cervical spondylosis, biliary heart syndrome, gastroesophageal reflux disease or esophageal hiatus hernia, neurosis, climacteric syndrome and other diseases related chest pain symptoms; 4. serum alanine aminotransferase or serum creatinine > 2 times the upper limit of normal reference value; 5. Patients with severe hematological diseases; 6. malignant tumors; 7. pregnant women, lactating women or women of childbearing age with fertility requirements; 8. Patients with psychotic or cognitive impairment; 9. allergy to the test drug; 10. those who have participated in other clinical trials within one month.

Design outcomes

Primary

MeasureTime frame
Electrocardiogram treadmill exercise test (metabolic equivalent);

Secondary

MeasureTime frame
ECG treadmill exercise test (duration of exercise test, depression time of exercise induced segment, positive condition of exercise test and maximum heart rate, maximum decrease of ST segment during exercise);Seattle Angina Scale;SF-36 QOL survey;TCM syndrome scores;Angina score;ECG;

Countries

China

Contacts

Public ContactJinjin Lu

Dongfang Hospital

13811678321@126.com+86 13811678321

Outcome results

None listed

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