Common antibiotic could shield hearts after attack
NCT ID NCT03508232
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a short course of doxycycline, a common antibiotic, can prevent heart damage after a heart attack. 174 adults who had a severe heart attack received either doxycycline or a placebo twice daily for one week. Researchers then used MRI scans to check heart structure three months later, hoping to see less scarring and better 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
- Doxycycline
- What this could lead to
- If it works, this could point toward a simple, short-term treatment to protect the heart after a heart attack and reduce the risk of future heart failure.
- What could go wrong
- This is a small pilot study, so results may not be conclusive. Doxycycline is not yet proven for this use, and the benefit may be small or absent.
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
-
Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
-
174 people
The number who actually took part.
- Started
-
Jan 2020
- Finished
-
Aug 2025
- Lead sponsor
-
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
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
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. 18+ year old 2. Diagnosis of acute ST-elevation myocardial infarction (STEMI) 3. Primary STEMI 4. Symptom onset of less than 12 hours 5. Admitted to the Royal Alexandra Hospital in Edmonton, Alberta Exclusion Criteria: 1. Low risk inferior STEMI (total ST elevation plus depression \<4mm) 2. Cardiogenic shock 3. Use of thrombolytics 4. Prior history of myocardial infarction or heart failure 5. Known hypersensitivity to tetracyclines 6. Any concurrent medical condition expected to reduce life expectancy to \<1 year 7. Symptom onset to treatment (loading dose) time longer than 24 hours 8. Poor renal function (eGFR\<30 mL/min/1.73m2) or other contraindications to MRI (claustrophobia, pregnancy, PPM/ICD, sub-arachnoid clips, retained ocular foreign body)
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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
-
Royal Alexandra Hospital
Edmonton, Alberta, T5H 3V9, Canada
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