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Clinical study on the early combined use of erlotinib and rosuvastatin in the treatment of patients with acute ST segment elevation myocardial infarction

Clinical study on the early combined use of erlotinib and rosuvastatin in the treatment of patients with acute ST segment elevation myocardial infarction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500099498
Enrollment
Unknown
Registered
2025-03-25
Start date
2023-07-23
Completion date
Unknown
Last updated
2025-03-31

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

Conditions

Acute ST segment elevation myocardial infarction

Interventions

Treatment group:On the basis of routine management, a subcutaneous injection of 140mg of erlotinib and 10mg of rosuvastatin were administered before PCI, followed by a change to 10mg qn.
Control group:Conventional treatment is given, including rosuvastatin 10mg, qn

Sponsors

Liaocheng People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age range: 18-75 years old; 2. Meets the diagnostic criteria for acute STEMI; 3. Successful completion of PCI within 12 hours of onset; 4. Have never used PCSK9 inhibitors in the past and have not taken statins within the 30 days prior to enrollment.

Exclusion criteria

Exclusion criteria: 1. Severe cardiac dysfunction or hemodynamic instability; 2. Combined with severe liver and kidney dysfunction; 3. Suffering from malignant tumors or inflammatory diseases; 4. Moderate to severe anemia: hemoglobin<90 g/L; 5. Statins cannot be tolerated or statin use is contraindicated. 6. Allergic to the medication required for this study. 7. I am currently participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Major cardiovascular adverse events (The composite endpoint includes death, recurrent myocardial infarction, unexpected revascularization, stroke, and readmission due to ischemia).;

Secondary

MeasureTime frame
Inflammation(Blood analysis, C-reactive protein, interleukin);ST segment regression on electrocardiogram;Left ventricular ejection fraction;Postoperative TIMI blood flow grading and myocardial color grading;Liver function;Renal function;Blood fat;

Countries

China

Contacts

Public ContactZuolin Fu

Liaocheng People's Hospital

13346253380@163.com+86 133 4625 3380

Outcome results

None listed

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