Ambulance steroid shot may cut heart attack deaths, large trial underway
NCT ID NCT07478003
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This phase 3 trial tests whether a single high dose of the steroid methylprednisolone, given in the ambulance before opening the blocked artery, can reduce deaths in people having a major heart attack (STEMI). About 5,200 adults will be randomly assigned to receive either the steroid or a placebo during transport. The main goal is to see if the treatment lowers the risk of dying from any cause over the following years.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Methylprednisolone (a steroid drug)
- What this could lead to
- If it works, this could become a standard prehospital treatment to reduce deaths and heart failure after a major heart attack.
- What could go wrong
- This is a large phase 3 trial, but earlier phase 2 results only showed trends, not proof. Steroids have risks like infection and may not improve survival.
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 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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About 5,204 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2026
- Expected to finish
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Apr 2036
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 including fertile women * Acute onset of chest pain with \< 24 hours duration * STEMI as characterized on electrocardiogram (ECG) by one of the following: 1. at least two contiguous leads with ST-segment elevation ≥2.5 mm in men \< 40 years, ≥2 mm in men ≥40 years, or ≥1.5 mm in women in leads V2-V3 and/or ≥1 mm in the other leads, 2. presumed new left bundle branch block with ≥1 mm concordant ST-segment elevation in leads with a positive QRS complex, or concordant ST-segment depression ≥1 mm in V1-V3, or discordant ST-segment elevation ≥5 mm in leads with a negative QRS complex 3. Isolated ST depression ≥0.5 mm in leads V1-V3 indicating posterior acute myocardial infarction (AMI) 4. ST-segment depression ≥1 mm in eight or more surface leads, coupled with ST-segment elevation in aVR and/or V1 suggesting left main-, or left main equivalent- coronary obstruction Exclusion Criteria: * Suspected other type I acute myocardial infarction at time of potential randomization * Initial presentation with cardiac arrest (out of hospital cardiac arrest) * Known allergy to glucocorticoid
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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
4 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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Aalborg University Hospital
NOT_YET_RECRUITINGAalborg, Denmark
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Odense University Hospital
NOT_YET_RECRUITINGOdense, Denmark
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Rigshospitalet
RECRUITINGCopenhagen, 2100, Denmark
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Skejby, Aarhus University Hospital
NOT_YET_RECRUITINGAarhus, Denmark
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Simple arm cuff before angioplasty may boost heart attack recovery
- Suction device may improve outcomes in heart attack patients with large clots
- AI blood test could spot heart attacks faster
- Heart attack patients may benefit from Clot-Busting drug before delayed procedure
- Heart attack patients to receive injectable gel that may limit damage