Skip to content

Clinical Study on the Improvement of Inflammatory Status after Interventional Surgery in Acute Myocardial Infarction with Phlegm Stasis Combined Treatment Formula

Clinical Study on the Improvement of Inflammatory Status after Interventional Surgery in Acute Myocardial Infarction with Phlegm Stasis Combined Treatment Formula

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400086906
Enrollment
Unknown
Registered
2024-07-15
Start date
2024-07-15
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

Coronary atherosclerotic heart disease

Interventions

treatment group:Conventional Western Medicine Treatment+Phlegm Stasis Combined Treatment Formula
Control group:Conventional Western Medicine Treatment+Placebo

Sponsors

Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of TCM
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Age = 18 years old and = 85 years old, gender not limited; 2. Meet the Western diagnostic criteria for acute myocardial infarction; 3. Complies with the phlegm blood stasis syndrome of coronary heart disease; 4. has undergone PCI surgery in the cardiology department of our hospital; 5. Voluntarily participate and sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Combined cardiogenic shock; 2. Patients Iwho are intolerant to statins and with severe liver and kidney dysfunction (ALT or AST = 2 times ULN, Cr>177umol/L); 3. Patients with old myocardial infarction, or with malignant tumor, serious infectious diseases, inflammatory disease, blood system disease, acute cerebral infarction, etc; 4. Pregnant or lactating women, or women of childbearing age who plan to conceive within the past 2 months; 5. Have taken or are currently taking traditional Chinese medicine of the same type as the phlegm and stasis treatment formula in the past three months; 6. Individuals who have participated or are currently participating in other clinical trials within the previous month.

Design outcomes

Primary

MeasureTime frame
hs-CRP;

Secondary

MeasureTime frame
Inflammatory factors;cardiac marker;blood lipids;

Countries

China

Contacts

Public ContactFan Min

Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of TCM

fanmin@medmail.com.cn+86 138 1883 5654

Outcome results

None listed

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