Cardiac MRI-guided Deferiprone Therapy for Acute Myocardial Infarction Patients
Recruiting now · Phase 2 · Has a placebo group
Conditions studied: Acute Myocardial Infarction Type 1
In brief
The objective of this randomized, controlled pilot study is to determine the efficacy of Deferiprone to reduce the amount of free iron inside the hemorrhagic zone of myocardial infarction among hemorrhagic myocardial infarction patients.
Key facts
- Study ID
- NCT05604131
- Run by
- Rohan Dharmakumar
- People needed
- 89
- Starts
- 2022-11-08
- Expected to finish
- 2029-08-31
- Last updated by the study team
- 2026-04-08
Who can join
Age: 18 and older, up to 79. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age 18-79 years
- Index Anterior wall STEMI
- Emergency coronary angiogram with primary PCI
You may not qualify if…
- Prior history of MI / PCI / coronary artery bypass graft (CABG) within previous 1 year
- Patients with previous history of left ventricular ejection fraction (LVEF) < 40%
- Use of investigational drugs or devices 30 days prior to randomization
- Known allergy or contra-indication to gadolinium/contrast agents
- eGFR < 30 ml/kg/min
- Any contraindication against cardiac MRI (such as metal implants)
- Women who are pregnant or breastfeeding. Women of reproductive potential must have a negative pregnancy test prior to randomization
- Body weight > 140 kg (or 309 lbs.)
- Absolute neutrophil count - ANC < 1.5 k/cumm
- History of Chronic Liver Disease
- Elevated hepatic enzymes (BOTH ALT and AST) > 2 times of upper normal limit
- Patients with iron storage disease (hemochromatosis, thalassemia) or who are already treated with iron chelators
- Any clinically significant abnormality identified prior to randomization that in the judgment of the Sponsor-Investigator or Delegate would preclude safe completion of the study or confound the anticipated benefit of deferiprone.
- Life expectancy of less than 1 year due to non-cardiac pathology
Where it is running
- IU Methodist Hospital (IUHealth) — Indianapolis, Indiana, United States (enrolling)
Full record on ClinicalTrials.gov
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