Cardiac MRI-guided Deferiprone Therapy for Acute Myocardial Infarction Patients
- Acute Myocardial Infarction Type 1
At a glance
- Phase
- Phase 2
- Study type
- Interventional
- Sponsor
- Rohan Dharmakumar
- Enrolment target
- 89
- Started
- 8 November 2022
- Main results due
- 31 March 2029
- Study sites
- 2
- Registry updated
- 29 September 2026
Can you take part?
- Aged 18 years and over.
- Open to any sex.
- You need the condition being studied — healthy volunteers are not accepted.
These are the headline rules only. Every study has a longer list, and whether you are eligible is decided by the research team at the site — never by this page.
Read the full eligibility criteria
Inclusion Criteria 1. At least 18 years of age 2. Index Anterior wall STEMI 3. Emergency coronary angiogram with primary PCI Exclusion Criteria 1. Prior history of MI / PCI / coronary artery bypass graft (CABG) within previous 1 year 2. Patients with previous history of left ventricular ejection fraction (LVEF) \< 40% 3. Use of investigational drugs or devices 30 days prior to randomization 4. Known allergy or contra-indication to gadolinium/contrast agents 5. eGFR \< 30 ml/kg/min 6. Any contraindication against cardiac MRI (such as metal implants) 7. Women who are pregnant or breastfeeding. Women of reproductive potential must have a negative pregnancy test prior to randomization 8. Body weight \> 140 kg (or 309 lbs.) 9. Absolute neutrophil count - ANC \< 1.5 k/cumm 10. History of Chronic Liver Disease 11. Elevated hepatic enzymes (BOTH ALT and AST) \> 2 times of upper normal limit 12. Patients with iron storage disease (hemochromatosis, thalassemia) or who are already treated with iron chelators 13. 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. 14. Life expectancy of less than 1 year due to non-cardiac pathology
What this study is about
In the sponsor’s own words, from the registry.
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.
Study sites(2)
IU Methodist Hospital (IUHealth)
Indianapolis, Indiana, United States
Recruiting
Minneapolis Heart Institute Foundation
Minneapolis, Minnesota, United States
Recruiting
Showing 2 of 2 sites. 2 of the 2 sites on this study are recruiting right now — a site can stop enrolling while the study as a whole is still open.
Source: ClinicalTrials.gov record NCT05604131. Trialion does not run this study, is not paid to refer anyone to it, and cannot enrol you. Eligibility is always decided by the research team at the site.
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