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Evaluation of the effect of colchicine on the frequency of ventricular and supraventricular arrhythmias

Evaluation of the effect of Colchicine on the frequency of ventricular and supraventricular arrhythmias in patients with an implantable cardioverter-defibrillator

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20120520009801N13
Enrollment
134
Registered
2024-06-01
Start date
2024-07-22
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

Ventricular arrhythmias. Re-entry ventricular arrhythmia

Interventions

Intervention 1: Intervention group: Intervention group:Colchicine 1 mg tablets, Mofid Pharmaceuticals, once a day for three months (67 people). Intervention 2: Control group: Control group: Placebo ta

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age more than 18 years Having an implantable cardioverter-defibrillator for more than 3 months before starting participation in the clinical trial Obtaining the patient's informed consent

Exclusion criteria

Exclusion criteria: Taking the drug Colchicine before Pregnancy or suspected pregnancy Active inflammation or infection Suffering from autoimmune diseases and malignancies Taking class I and III antiarrhythmic drugs Performing major surgeries Treatment with corticosteroids or other immunosuppressive drugs Moderate to severe kidney dysfunction (GFR < 30 ml/min/1.73m2) Significant impairment of liver function (Child-Pugh class B or C) Concomitant use of strong Cyp3A4 inhibitors

Design outcomes

Primary

MeasureTime frame
Frequency of ventricular arrhythmias. Timepoint: The beginning of the study and 3 months later. Method of measurement: Examining the data obtained from the implantable cardiac defibrillator device.

Secondary

MeasureTime frame
CRP level. Timepoint: Before the intervention and after 3 months. Method of measurement: Biochemistry test of the patient's blood sample.;Blood pressure. Timepoint: Before the intervention and after 3 months. Method of measurement: sphygmomanometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAmir Hooshang Mohammadpour

Mashhad University of Medical Sciences

mohamadpoorah@mums.ac.ir+98 51 1882 3255

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026