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Research and development of traditional Chinese medicine preparations in medical institutions

Research and development of traditional Chinese medicine preparations in medical institutions

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025000487
Enrollment
Unknown
Registered
2025-03-07
Start date
2024-12-03
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

Coronary heart disease with heart failure

Interventions

Treatment group:Qiyi granules formula + conventional treatment of Western medicine

Sponsors

Jiangsu Province Hosptial of Chinese Medicine Affiliated Hosptial of Nanjing University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Those who meet the diagnosis of coronary heart disease NYHA cardiac function classification: grade II-III LVEF <50% measured by echocardiography and blood BNP/NT-proBNP elevation meets the standard. 2. It is in line with the syndrome type of qi and yin deficiency and phlegm stasis and paralysis in traditional Chinese medicine. 3. Age between 18~80 years old gender is not limited. 4. Informed consent voluntary test. The process of obtaining informed consent should be in accordance with GCP regulations.

Exclusion criteria

Exclusion criteria: 1. Combined with severe heart valve disease and myocarditis. 2. Combined with malignant tumors connective tissue diseases rheumatic immune system diseases and hematologic diseases. 3. Asthma chronic obstructive pulmonary disease and severe acute and chronic infectious diseases. 4. Patients with severe liver and kidney insufficiency. 5. Pregnant or lactating females. 6. Uncontrollable mental illness. 7. Those with unclear ultrasound images. 8. Suspected or confirmed history of alcohol and drug abuse. 9. According to the judgment of the investigator there are other pathologies that reduce the possibility of enrollment or complicate enrollment such as frequent changes in the working environment and other conditions that are easy to cause loss to follow-up. 10. Allergies such as a history of allergies to two or more drugs or food; or those who are known to be allergic to the ingredients of this medicine. 11. Patients who are participating in clinical trials of other drugs.

Design outcomes

Primary

MeasureTime frame
Routine echocardiography;Analysis of 2D speckle tracking imaging techniques;Brain Natriuretic Peptide;

Secondary

MeasureTime frame
TCM symptom efficacy indicators;

Countries

China

Contacts

Public ContactLingzhun Wang

Jiangsu Province Hosptial of Chinese Medicine Affiliated Hosptial of Nanjing University of Chinese Medicine

lzwangdd@sina.com13645187394

Outcome results

None listed

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