Heart attack drug targets tiny vessels, not blockages
NCT ID NCT05198791
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This trial tests whether eplerenone, a drug used for high blood pressure and heart failure, can help people who have had a heart attack or heart injury but no blocked arteries. Many of these patients have damage to tiny blood vessels in the heart. The study will involve 400 adults in Scotland. Participants with small vessel problems will either get eplerenone or usual care for six months. The main goal is to see if the drug reduces heart injury markers and improves heart function.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Eplerenone (a tablet that reduces blood vessel injury, used for high blood pressure and heart failure)
- What this could lead to
- If it works, this could point toward a treatment for heart damage caused by small vessel problems after a heart attack.
- What could go wrong
- This is an early phase 2 trial with only 400 participants, so results may not apply to everyone. The drug may not reduce heart injury or improve outcomes as hoped.
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.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 400 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2022
- Expected to finish
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Jul 2026
An estimate. End dates often move.
- 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.
- 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: * Age ≥18 years. * Acute myocardial infarction or myocardial injury and no obstructive coronary arteries. * Cardiovascular risk factor (≥1): age \>70 years, atrial fibrillation, diabetes, current smoker, eGFR 30 - 60 mL/ minute/1.73 m2, prior MI, treated hypertension or COVID-19 (confirmed or suspected) * Coronary angiography. Exclusion Criteria (trial): * Obstructive coronary artery disease * Left ventricular ejection fraction ≤40% with evidence of heart failure, following myocardial infarction. * Estimated glomerular filtration rate \<30 mL/ minute/1.73 m2 * Severe liver impairment * Women who are pregnant, breast-feeding or of child-bearing potential (WoCBP) without a negative pregnancy test and who are unwilling or unable to follow the reproductive restrictions defined in the eligibility criteria and use highly effective contraception as defined in Appendix 2 for the duration of the study treatment and 30 days after last dose of study drug. * Patients taking one of the following medicines : * Pre-existing treatment with an MRA : * Anti-fungal drugs (ketoconazole or itraconazole). * Antiviral medication (nelfinavir or ritonavir). * Antibiotics (clarithromycin or telithromycin). * Nefazodone used to treat depression. * The combination of an angiotensin converting enzyme (ACE) inhibitor and an angiotensin receptor blocker (ARB)) together. Exclusion Criteria (registry): * Contra-indication to cardiovascular magnetic resonance imaging e.g. severe claustrophobia, metallic foreign body. * Contra-indication to intravenous adenosine, i.e. severe asthma; long QT syndrome; second- or third-degree atrio-ventricular block and sick sinus syndrome. * Lack of informed consent.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
2 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Golden Jubilee National Hospital
RECRUITINGGlasgow, United Kingdom
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University Hospital Hairmyres
RECRUITINGEast Kilbride, Lanarkshire, G75 8RG, United Kingdom
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