Effect of Pentoxifylline in improvement Myocardial Injury in Patients with ST-elevation myocardial infarction treated by primary percutaneous coronary interventio
- Conditions
- Myocardial infarction.ST elevation (STEMI) myocardial infarction of unspecified siteI21.3
- Registration Number
- IRCT20240323061353N1
- Lead Sponsor
- Bagheiat-allah University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 70
Diagnosis of STEMI, as chest pain lasting more than 30 minutes and less than 12 hours with ST-segment elevation at the J point on the ECG for more than 1 mm in at least two consecutive leads
Precancerous coronary intervention successful
sinus rhythm
Informed consent to participate in the study
Recent history (within 3 months) of coronary artery bypass grafting
Receive thrombolytic therapy
Recent electrophysiological interventions of the heart
Cardiogenic shock at the time of presentation
History of kidney failure (Creatinine > 2.5 mg/dL)
Allergy and contraindication to aspirin, clopidogrel or pentoxifylline
Those who are pregnant or breastfeeding
Dissatisfaction and those who want to stop the study at any time
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Troponion I. Timepoint: Upon entering the emergency room and then 8, 16 and 32 hours after revascularization treatment. Method of measurement: Blood test.;Interleukin 6. Timepoint: On arrival in the emergency room and 48 hours and 15 days after revascularization treatment. Method of measurement: Blood Test.;Hs-CRP. Timepoint: On arrival in the emergency room and 48 hours and 15 days after revascularization treatment. Method of measurement: Blood test.;CPK. Timepoint: On arrival to the emergency department as a baseline sample and every 8 hours to 48 hours after revascularization treatment. Method of measurement: Blood test.
- Secondary Outcome Measures
Name Time Method