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Study on the clinical efficacy and mechanism of improving endothelial diastolic function of blood vessels in the treatment of coronary heart disease with qi stagnation in the heart and chest by regulating liver and promoting yang

A randomized, double-blind, placebo-parallel-controlled clinical trial to evaluate the safety and clinical efficacy of the Liver-Tong Yang method in the treatment of coronary heart disease with Qi stagnation in the heart and chest

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200065514
Enrollment
Unknown
Registered
2022-11-07
Start date
2021-05-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Coronary heart disease

Interventions

Treatment group:Conventional western medicine + Chai Hu Gui Zhi Tang granules
Control group:Conventional western medicine+Placebo granules

Sponsors

Yueyang Hospital of Integrative Medicine, Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1 Meet the diagnostic criteria for stable angina pectoris in coronary heart disease. 2 Meeting the diagnostic criteria of TCM chest paralysis - Qi stagnation in the heart and chest. 3 Subjects were between the ages of 40 and 80 years, including 40 and 80 years, with no restriction on gender. 4 Subjects gave informed consent to participate in this study, signed an informed notification form and were able to cooperate with the treatment

Exclusion criteria

Exclusion criteria: 1 Those with confirmed acute myocardial infarction (including necrotic Q-wave and non-necrotic Q-wave types), unstable angina pectoris, and chest pain due to e.g. hyperthyroidism, menopausal syndrome, biliary heart disease, neurosis, gastric and esophageal reflux, neuritis, trauma, etc. 2 with factors such as severe heart failure, cardiogenic shock, severe ventricular arrhythmias, obstructive or dilated cardiomyopathy, pericardial tamponade, severe hemodynamically unstable heart valve disease, pulmonary embolism, uncontrollable hypertension, and severe infections. 3 Patients who meet the diagnostic criteria for stable angina pectoris in coronary artery disease but are not routinely treated according to the relevant guidelines. 4 Patients with serious combined diseases of the liver, kidney, hematopoietic system and endocrine system. 5 Patients with psychiatric abnormalities and unwillingness to cooperate 6 Pregnant or lactating women or women with childbearing requirements 7 Allergy or multiple drug allergy. 8 Other conditions deemed by the investigator to be unsuitable for participation in this trial

Design outcomes

Primary

MeasureTime frame
Angina pectoris treatment effect;Chinese medicine evidence of efficacy;

Secondary

MeasureTime frame
Nitroglycerin discontinuation reduction rate;Resting ECG Efficacy;Seattle Angina Scale;Blood lipids;Vascular endothelial diastolic function index;

Countries

China

Contacts

Public ContactShen Yan
sheny26@126.com18930568212

Outcome results

None listed

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