Heart attack drug trial halted early: Colchicine's nerve protection unproven
NCT ID NCT04420624
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether the anti-inflammatory drug colchicine could prevent nerve damage in the heart after a heart attack. About 54 adults who had a first heart attack and underwent artery-opening treatment were given colchicine or a placebo for one month. The trial was terminated early, so it is unclear if colchicine provides any benefit for this purpose.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- colchicine
- What this could lead to
- If it had worked, this could point toward a way to reduce heart nerve damage after a heart attack.
- What could go wrong
- The study was terminated early with only 54 participants, so we don't have enough data to know if colchicine helps. It was also a small, early-phase trial.
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 2/3
Runs two stages together: whether the treatment works, then large-scale confirmation.
- Participants
-
54 people
The number who actually took part.
- Started
-
Dec 2020
- Finished
-
May 2022
- 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 to 80 years
- 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: * Age from 18 to 80 year old * Hospitalization within 12 hours of onset of acute chest pain * Patient must have suffered a documented acute myocardial infarction * Coronary occlusion on initial angiography (culprit artery with aTIMI (Thrombolysis in Myocardial Infarction) flow 1 or 0) * Patient eligible for a revascularization procedure by PTCA (Percutaneous transluminal coronary angioplasty) Exclusion Criteria: * Patients with a history of myocardial infarction prior to the current episode * Patient in cardiogenic shock or with hemodynamic instability * Patients with severe hepatic or renal dysfunction (GFR ≤30 mL/min) * Pregnant women or women of childbearing age without contraception * Treatment with a potent CYP3A4 inhibitor or a P-glycoprotein inhibitor in patients with renal or hepatic impairement * Association with macrolides (except spiramycin) * Association with pristinamycin
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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
-
UH Montpellier
Montpellier, 34090, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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