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Evaluation of the efficacy and safety of colchicine in the prevention for post-CABG atrial fibrillation

Evaluation of the efficacy and safety of colchicine in the prevention for post-CABG atrial fibrillation: a randomized double-blind placebo- controlled trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200328046886N6
Enrollment
172
Registered
2024-07-25
Start date
2024-07-22
Completion date
Unknown
Last updated
2024-08-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atrial Fibrillation. Unspecified atrial fibrillation

Interventions

Intervention 1: Intervention group: Patients in the intervention group will be given orally 1 mg of colchicine every 12 hours 24 hours before surgery, then 0.5 mg daily if they weigh less than 70 kg o

Sponsors

Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patient between 18_80 years old Patient with CAD and candidate for CABG

Exclusion criteria

Exclusion criteria: Preoperative AF Patients with pacemakers Patient with Clcr<30ml/min Severe hepatic insufficiency or transaminase level more than 3 times higher than normal Breastfeeding or pregnancy Colchicine intolerance or allergy Lack of patients consent to participate in study Presences of sick Sinus syndrom Previous cardiac rhythm disorder,conduction blocks of any degree Co administration with strong pgp and 3A4 inhibitors (voiconazol,ketoconazole,fluconazole,itraconazole,clarithromycin,etc.) Taking anti arrhythmic medicines except beta blockers during past months of surgery

Design outcomes

Primary

MeasureTime frame
Atrial fibrilation. Timepoint: Monitoring up to 14 days. Method of measurement: ECG.

Secondary

MeasureTime frame
Duration of hospitalization. Timepoint: From CABG surgery to hospital discharge. Method of measurement: Monitoring.;Inflammatory factors (CRP,IL6). Timepoint: Day 1 and day 7. Method of measurement: Blood test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHamideh Abbaspour Kasgari

Mazandaran University of Medical Sciences

dr.abbaspour1@yahoo.com+98 11 4203 1035

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: May 16, 2026