RecruitingPhase 3NCT05928728

The COLchicine and Atrial FIBrillation Trial

The Colchicine and Atrial Fibrillation Trial

Sponsor

Herlev and Gentofte Hospital

Enrollment

500 participants

Start Date

Jul 3, 2023

Study Type

INTERVENTIONAL

Conditions

Atrial Fibrillation

Summary

The purpose of this study to investigate the effects of colchicine on atrial fibrillation recurrence and vascular and cardiac function in patients with atrial fibrillation.

Eligibility

Min Age: 18 Years

Inclusion Criteria7

Living address in the Capital Region of Denmark
Age \> 18
Diagnosed with paroxysmic/persistent AF.
Planned or acute admission for cardioversion of AF with successful outcome.
Female participants should either not be of childbearing potential, defined as postmenopausal for at least 1 year or surgically sterile, or is of childbearing potential and practicing one of the following methods of contraception throughout the study and for 30 days after study completion: Hormonal contraception (oral contraceptives, contraceptive implant, injectable birth control, contraceptive patch, or vaginal ring) or intrauterine device
Participants will have given written, informed consent and are able and willing to comply with the requirements of the study protocol.
Optimal background therapy (in relation to comorbidities and development of heart failure / thromboembolic event) for AF as judged by the investigator.

Exclusion Criteria18

Colchicine treatment for another cause, e.g. gout
Allergy/hypersensitivity to colchicine
Uncontrolled hypertension (systolic BP \>180 mmHg or diastolic BP \>110 mmHg)
History of malignancy of any organ system excluding a successfully treated non-metastatic cutaneous squamous cell or basal cell carcinoma, localized prostate cancer and/or localized carcinoma in situ of the cervix
Cirrhosis, chronic active hepatitis or other severe hepatic disease
Hemodialysis
Estimated glomerular filtration rate (eGFR) \< 60 mL/min/1.73 m2
Systemic treatment with moderate or strong cytochrome P450 3A4 (CYP3A4) inhibitors or P-glycoprotein inhibitors (list in Appendix 1)
Permanent AF
Female participants who are pregnant, lactating, or considering becoming pregnant during the study or for 6 months after study completion
Significant drug or alcohol abuse during the last year
Current use of or plans to initiate chronic systemic steroid therapy during the study (topical or inhaled steroids are allowed)
Planned ablation procedure as treatment for AF
If cardiovascular surgery or ablation has been done the past three months prior to inclusion.
Chronic inflammatory bowel disease (Crohn's disease or ulcerative colitis) or chronic diarrhea
Use of other investigational drugs within 30 days of the time of enrollment
Any surgical or medical condition, which in the opinion of the investigator, may place the patient at higher risk from his/her participation in the study, or is likely to prevent the patient from complying with the requirements of the study or completing the study.
Suspected AF, confirmed with ECG, at time of inclusion and randomization