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Colchicine Versus Placebo in Acute Myocarditis Patients to Reduce Late Gadolinium Enhancement Mass on Cardiac Magnetic Resonance and the Risk of Clinical Outcomes: The ARGO Trial

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

Myocarditis is an inflammatory disease of the heart, mostly caused by viruses. Patients with acute myocarditis are exposed to several complications: recurrence, ventricular arrhythmias (from 5 to 30%), heart failure (5-10%), death or heart transplantation (\< 4%). To date, there is no specific treatment for myocarditis. Patient management only focuses upon empirical optimal care of arrhythmia and heart failure. There is a strong rationale for using colchicine in acute myocarditis: * the IL1 (Interleukin1) pathway plays a detrimental role in acute myocarditis. NLRP3 (NOD-like receptor family, pyrin domain containing 3) inflammasome assembly, and subsequent IL-1beta production, are profoundly inhibited by colchicine. * colchicine has been shown to improve cardiac outcomes in inflammatory cardiac disorders, including pericarditis, coronary artery disease, and post pericardiotomy syndrome. * In murine model of CVB3-induced myocarditis (coxsackievirus B3), colchicine improved myocarditis through reduction of NLRP3 activity. * Small case series with improvement of left ejection fraction in myocarditis following low-dose colchicine in addition to conventional heart failure therapy have been reported. With its pleiotropic anti-inflammatory effect in the pro-inflammatory cascade, reducing the myocardial damage and cell death induced during myocarditis, colchicine has the potential to reduce the risk of heart failure and ventricular arrhythmias. Finally, colchicine is a drug widely available, at low cost, and has a long and well-known safety record.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• Symptom onset of 28 days or less,

• Myocarditis initially presenting with chest pain and/or Heart failure symptoms and/or palpitations

• Troponins superior to 99 percentile of reference value, at any time between admission and inclusion

• Myocarditis diagnostic confirmation (by Contrast-Enhanced Cardiac Magnetic Resonance (CMR), according to the Lake Louise criteria (2009 or later),

• No evidence for ischemic heart disease on coronary angiography or coronary computed tomography angiography for patients with age superior to 40-year-old with one or more cardiovascular risk factor (hypertension, smoking, hypercholesterolemia, diabetes, personal or family history of coronary artery disease),

• Woman of child-bearing age with an effective contraception method according to the investigator for the duration of treatment and one month after,

• Man accepting effective contraception for the duration of treatment and one month after,

• Participant with affiliation to the French Health Care System sécurité sociale,

• Written informed consent of the patient obtained.

Locations
Other Locations
France
Unité de Soins Intensifs Cardiologiques - Hôpital Cardiovasculaire Louis Pradel
RECRUITING
Bron
Institut de Cardiologie - APHP Pitié Salpêtrière
RECRUITING
Paris
Contact Information
Primary
Thomas BOCHATON
thomas.bochaton@chu-lyon.fr
+33472357549
Backup
Julia CANTERINI
julia.canterini@chu-lyon.fr
+33427856628
Time Frame
Start Date: 2024-07-16
Estimated Completion Date: 2028-07-16
Participants
Target number of participants: 300
Treatments
Experimental: Colchicine
Participant receive in addition to standard of care therapy, six months of Colchicine
Placebo_comparator: Placebo
Participant receive in addition to standard of care therapy, six months of placebo
Sponsors
Collaborators: Hospices Civils de Lyon, Fonds de Dotation ACTION
Leads: Assistance Publique - Hôpitaux de Paris

This content was sourced from clinicaltrials.gov