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Development of a Formulation for Treating Coronary Heart Disease and Angina Pectoris with Ningxin Drink

Development of a Formulation for Treating Coronary Heart Disease and Angina Pectoris with Ningxin Drink

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025000482
Enrollment
Unknown
Registered
2025-03-06
Start date
2025-03-15
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Unstable Angina Pectoris of Coronary Heart Disease

Interventions

Standard Intensive Western Medical Therapy Group:Standard Intensive Western Medical Therapy, with a conventional treatment regimen including: Anti-myocardial ischemia therapy,Antiplatelet aggregation
Treatment Group:Ningxin Yin Herbal Formula

Sponsors

Nan Jing Hospital of C.M.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Meet the diagnostic criteria for coronary atherosclerotic heart disease in Western medicine. Coronary angiography (CAG) or coronary computed tomography angiography (CTA) reveals at least one epicardial coronary artery with a diameter stenosis exceeding 50%; or a clear history of myocardial infarction with resting electrocardiogram (ECG) showing evidence of a past myocardial infarction; or a history of revascularization [percutaneous coronary intervention (PCI) or coronary artery bypass grafting (CABG)]. 2.Meet the diagnostic criteria for unstable angina pectoris in Western medicine (including new-onset exertional angina worsening angina or spontaneous angina) classified as intermediate or low risk. 3.Meet the diagnostic criteria for the traditional Chinese medicine (TCM) syndrome of "chest obstruction and heart pain" (). 4.Meet the TCM syndrome diagnostic criteria for "phlegm-stasis obstruction syndrome" () as defined in this research study. 5.Age =18 and =75 years old; gender is not restricted. 6.Patients who do not currently plan to undergo revascularization (PCI or CABG). 7.Patients voluntarily agree to participate in this clinical study and sign a written informed consent form.

Exclusion criteria

Exclusion criteria: 1.Patients confirmed by examination to have acute myocardial infarction due to coronary heart disease unstable angina with high-risk stratification or chest pain caused by other cardiac conditions cardiac neurosis menopausal syndrome or cervical spondylosis. 2.Patients with severe cardiopulmonary insufficiency severe arrhythmias severe primary diseases of the liver kidneys or hematopoietic system or psychiatric disorders. 3.Pregnant or breastfeeding women. 4.Patients with a known allergy to the study medication. 5.Patients who are planning to immediately undergo revascularization (PCI or CABG).

Design outcomes

Primary

MeasureTime frame
Changes in Serum TC, LDL-C, and TG Levels;Change in the Reduction or Discontinuation Rate of Sublingual Nitroglycerin Tablets;

Secondary

MeasureTime frame
Changes in TCM Syndrome Scores and Therapeutic Efficacy;The study evaluated the therapeutic efficacy of TCM "chest obstruction" symptoms, including the frequency, severity, duration, triggers, and changes in accompanying symptoms of angina pectoris.;Liver Function Tests, Renal Function Tests, Blood Glucose, and Routine Blood, Urine, and Stool Tests;Changes in ECG Results;Change in cTnI Levels ;

Countries

China

Contacts

Public ContactHuang Xia

Nan Jing Hospital of C.M.

510807540@qq.com13776684529

Outcome results

None listed

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