Ultrasound 'Memory' imaging may reveal hidden heart ischemia
NCT ID NCT07762495
First seen Aug 13, 2026 · Last updated Aug 21, 2026 · Updated 3 times
Summary
This trial tests whether a special ultrasound technique can detect heart muscle ischemia (reduced blood flow) in people with suspected acute coronary syndrome. The approach uses microbubbles that stick to activated immune cells and blood vessel linings, potentially revealing inflammation even after the ischemia has resolved. Researchers will compare the imaging results with a final diagnosis made by an expert committee to see how accurate the test is.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Myocardial contrast echocardiography (MCE) molecular imaging with Sonazoid, a contrast agent containing microbubbles designed to stick to activated immune cells and blood vessel linings to reveal inflammation from ischemia.
- What this could lead to
- If it works, this could lead to a quick, bedside ultrasound test that helps doctors rapidly confirm or rule out a heart attack, potentially speeding up treatment and reducing unnecessary hospital stays.
- What could go wrong
- This is an early, proof-of-concept study with a small number of patients, so the imaging may not be accurate enough for routine use. There is also a small risk of allergic reactions to the contrast agent.
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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Early phase 1
The earliest testing in people: a first look at safety, in a very small group.
- Participants
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About 80 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Jul 2030
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 to 99 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.
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 of age * Patients with possible or suspected ACS based on clinical criteria (history, ECG, laboratories) and HEART score \>3. Exclusion Criteria: * Cardiogenic shock * Inability to obtain consent * Severe heart failure (NYHA class IV) * Mechanical complication of MI (ischemic VSD, papillary muscle rupture, ventricular free wall rupture) * Ongoing life-threatening arrhythmias * Neutropenia (\<1,500/mm3) * Pregnancy * Lactation * Allergy to ultrasound contrast agents or eggs * History of autoimmune or inflammatory disease with myocardial involvement (SLE, sarcoidosis, giant cell myocarditis, etc.)
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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
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.
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