Heart attack drug may fix 'Hidden' vessel damage
NCT ID NCT06787430
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether the drug nicorandil can improve blood flow in the heart's tiny vessels after a heart attack. About 170 patients having emergency angioplasty will receive either nicorandil or a placebo directly into their heart artery. The goal is to see if nicorandil reduces microvascular dysfunction, a common problem that can lead to worse outcomes.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- nicorandil
- What this could lead to
- If it works, this could point toward a simple, cheap way to improve blood flow in the heart's tiny vessels after a heart attack, potentially reducing long-term damage.
- What could go wrong
- This is a relatively small, early-phase trial testing a short-term drug effect. The benefit may be small or not translate to better long-term outcomes, and the drug can cause low blood pressure.
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 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
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About 170 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Mar 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a government body.
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 to 80 years
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age between 18-80 * Diagnosis of STEMI and indicating for primary PCI * Diagnostic coronary angiography showed definite culprit vessel and primary PCI was planned to treat the culprit vessel. * Reference vessel diameter of culprit vessel was greater than 2.0 mm * There was no flow-limiting stenosis for the non-culprit vessels. * Understand the aim of this trial and agree to sign the informed consent form. Exclusion Criteria: * Acute in- stent thrombosis or in-stent stenosis lesions of culprit vessel. * Balloon angioplasty rather than stent was planned for the culprit vessel. * Allergic to nicorandil or systolic arterial pressure was less than 85mmHg before procedure * Vessel with twisted shape that was unable to be measured using AMR * Oral or intravenous use of nicorandil within one month. * Cardiac shock needing mechanical support. * Severely hepatic dysfunction. * Severely renal failure needing hemodialysis. * Contraindicated for coronary angiography or primary PCI. * Culprit vessels of left main or graft vessels. * Pregnant or nursing. * Others that investigators think should excluded.
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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 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
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