Effect of L-Carnitine on Biomarkers of Myocardial Reperfusion Injury in Patients With STEMI
Recruiting now · Phase 2
Conditions studied: Reperfusion Injury, Myocardial, Myocardial Infarction
In brief
The study aims is to evaluate the efficacy and tolerability of L-Carnitine on biomarkers of myocardial reperfusion injury in patients with ST-segment elevation myocardial infarction (STEMI) undergoing primary PCI by the assessment of nitrotyrosine as an oxidative stress marker and Matrix metallopeptidase-2 (MMP-2) as a cardiac fibrosis marker
Key facts
- Study ID
- NCT06564909
- Run by
- Ain Shams University
- People needed
- 76
- Starts
- 2025-06-01
- Expected to finish
- 2026-03-01
- Last updated by the study team
- 2025-06-26
Who can join
Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Female or male aged >18 and < 75 years.
- STEMI patients undergoing PCI.
You may not qualify if…
- Patients with a recent history of myocardial infarction (MI), a previous PCI, a previous coronary artery bypass graft, or any cardiac surgery.
- A late presentation (>12 h), unsuccessful primary PCI (residual stenosis >50% in the culprit lesion after procedure),
- Pretreatment with thrombolytic or glycoprotein IIb/IIIa inhibitor therapy before primary PCI,
- Concurrent Infectious or active inflammatory disease,
- Severe liver or renal disease, (aspartate aminotransferase (AST) or alanine transaminase (ALT) > 3x ULN or Total bilirubin > 3 x ULN), (CrCl < 60 ml/min (based on the Cockroft-Gault equation)
- Neoplasm, or hematological disorders
- Pregnant or breast-feeding patients
- Active participation in another clinical study
- Patients taking antioxidant drugs.
- History of or known allergy or intolerability to the study medications
Where it is running
- Ain Shams University Hospitals — Cairo, Egypt (enrolling)
Full record on ClinicalTrials.gov
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