CHIP in STEMI: Does clonal hematopoiesis influence infarct severity
Official title: Clonal Hematopoiesis of Indeterminate Potential and Infarct Severity in ST-Elevation Myocardial Infarction
Run by Medical University Innsbruck · NCT07615023 · Data updated 2026-11-12
This study tests whether clonal hematopoiesis (CHIP) affects infarct size and microvascular injury in people having a heart attack treated with PCI.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 75 Years |
| Sex | All |
| Enrollment | 350 (estimated) |
| Sponsor | Medical University Innsbruck Academic / other |
| Drugs / interventions | chemotherapy |
| Locations | 1 site (Innsbruck, Tyrol) |
| Status | Recruiting |
| Started | June 20, 2026 |
| Main results expected | June 20, 2029 |
| Study ends | June 20, 2030 |
| Registry record updated | October 9, 2026 |
| Trial ID | NCT07615023 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults 18-75 with first STEMI treated with successful primary PCI within 12 hours of symptom onset and able to undergo cardiac MRI.
✕Probably not a fit
Patients with prior myocardial infarction, known hematologic malignancy, significant MRI contraindications, or life expectancy <12 months may not benefit from this observational study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is a prospective, observational cohort study at a single center aiming to enroll 350 adults aged 18-75 with STEMI treated by primary PCI. Participants will undergo genetic testing for CHIP mutations and a cardiac MRI about 5 days after PCI to measure microvascular obstruction, intramyocardial hemorrhage, and infarct size, along with ventricular function. The study explores whether CHIP-associated inflammation contributes to worse ischemia–reperfusion injury beyond standard care. No experimental intervention is given; all care remains standard. Data will be used to understand potential links between CHIP and adverse cardiac remodeling after STEMI.
Why it matters
Potential benefit: If CHIP is linked to worse infarct outcomes, findings could guide risk stratification and future therapies targeting inflammation after STEMI.
How similar studies have gone: Previous work shows CHIP associates with higher cardiovascular risk, but data specifically linking CHIP to STEMI infarct severity are limited, making this approach exploratory.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Diagnosis of first acute ST-elevation myocardial infarction according to current European Society of Cardiology guidelines * Symptoms consistent with ST-elevation myocardial infarction lasting more than 30 minutes and less than 12 hours before primary percutaneous coronary intervention * Treatment with primary percutaneous coronary intervention * Age 18 to 75 years * Written informed consent Exclusion Criteria: * Prior myocardial infarction, coronary artery bypass grafting, or percutaneous coronary intervention * Persistent hemodynamic instability, Killip class greater than 2 including cardiogenic shock, or resuscitated cardiac arrest not allowing cardiac magnetic resonance imaging * Known active or prior malignancy, including hematologic malignancies or myelodysplastic syndromes * Prior oncologic treatment with chemotherapy, radiotherapy, or radioisotopes * Abnormal baseline complete blood count with clinically significant cytopenia, defined as leukocytes less than 3.0 x 10\^9/L, platelets less than 100 x 10\^9/L, or hemoglobin less than 10 g/dL * Chronic viral infection associated with systemic inflammation * Active autoimmune disease or chronic systemic inflammatory disorder * Chronic kidney disease with creatinine clearance less than 30 mL/min/1.73 m2 * Contraindication to cardiac magnetic resonance imaging * Pre-ST-elevation myocardial infarction life expectancy of less than 1 year * Participation in an interventional trial * Limited possibility to attend follow-up examinations, for example residence abroad * Pregnancy
Where it's running
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Medical University of Innsbruck
Innsbruck, Tyrol, Austria Recruiting
Study contacts
- Study coordinator: Ivan Lechner, MD, PhD
- Email: ivan.lechner@tirol-kliniken.at
- Phone: +43 512 504 83772
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.