Simple blood test may spot hidden bleeding in heart attacks
NCT ID NCT05872308
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This pilot study tested whether a common blood test for troponin, a heart damage marker, can tell if a heart attack involves bleeding in the heart muscle. Researchers measured troponin levels in 227 patients after they had a heart attack and compared those with and without bleeding seen on MRI. The goal is to develop a non-invasive way to detect hemorrhagic myocardial infarction, which may require different treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could lead to a simple blood test to identify which heart attack patients have bleeding in the heart, guiding more personalized treatment.
- What could go wrong
- This is a small, completed pilot study. The findings need confirmation in larger trials before changing clinical practice.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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227 people
The number who actually took part.
- Started
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Jul 2022
- Finished
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Jan 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The study population consists of individuals aged 18 to 80 who have been diagnosed with acute ST-elevation myocardial infarction (STEMI) and are scheduled for emergency percutaneous coronary intervention (PCI).
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Age ≥ 18 years 2. Index STEMI 3. Coronary angiogram with PCI to occur irrespective of the onset of the symptoms. 4. Ability to provide informed consent for themselves Exclusion Criteria: 1. History of prior myocardial infarction, 2. Cardiogenic shock, 3. Patients who present with current cardiac arrest 4. Any contraindication to cardiac CMR (claustrophobia, pacemaker or cardiac defibrillator, known allergy to gadolinium), 5. Presence of permanent atrial fibrillation, 6. Unconscious patient, 7. Severe renal insufficiency (creatinine clearance ≤ 30 ml/min/m2 or renal replacement therapy), 8. Women who are pregnant or breastfeeding. Women of reproductive potential must have a negative pregnancy test.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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IU Methodist Hospital
Indianapolis, Indiana, 46202, United States
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Synergy Cardiovascular Research Center, Synergy Superspecialty Hospital
Rajkot, Gujarat, India
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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