Heart surgery patients get new hope: colchicine may stop Post-Op AFib
NCT ID NCT06798714
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study tests whether the anti-inflammatory drug colchicine, combined with a special surgical technique, can prevent atrial fibrillation (a type of irregular heartbeat) after coronary artery bypass surgery. Researchers will compare 70 patients receiving colchicine plus the new technique against 70 patients getting standard care. The goal is to reduce dangerous heart-rhythm problems after surgery.
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 works, this could offer a simple, low-cost way to prevent a common heart-rhythm problem after bypass surgery.
- What could go wrong
- This is a small, early-phase trial with only 140 people, so results may not apply to everyone. Colchicine can cause stomach upset or other side effects.
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 140 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2025
- Expected to finish
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Feb 2026
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: 1. Elective coronary artery bypass grafting on pump; 2. signed informed consent to participate in the study. Exclusion Criteria: 1. Reduced left ventricular ejection fraction (≤35%); 2. Valvular heart disease requiring surgical correction; 3. Liver failure with an increase in liver transaminases ≥1.5 times; 4. Renal failure (GFR\<35 mL/min/1.73 m2 calculated with CKD-EPI); 5. Permanent, persistent or paroxysmal atrial fibrillation; 6. Previously implanted pacemaker; 7. Hypersensitivity to colchicine; 8. Neutropenia; 9. History of alcoholism; 10. Refusal to sign informed consent
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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
1 site. 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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Cardiology Research Institute, Tomsk National Research Medical Center, Russian Academy of Sciences, Tomsk, Russia
RECRUITINGTomsk, 634012, Russia
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