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Blockade of the Renin-angiotensin-aldosterone System in Patients With ARVD
Sponsor: Hospices Civils de Lyon
Summary
Arrhythmogenic right ventricular dysplasia (ARVD) is a rare cardiomyopathy characterized by the progressive replacement of cardiomyocytes by fatty and fibrous tissue in the right ventricle (RV). These infiltrations lead to cardiac electrical instability and ventricular arrhythmia. Current treatment for ARVD is empirical and essentially based on treatment of arrhythmia. Thus, there is no validated treatment that will prevent the deterioration of the RV function in patients with ARVD. The investigator's hypothesis is that the use of anti-fibrotic medications will prevent or at least reduce the deterioration of the RV function. The aim of this project is to evaluate the effect of spironolactone, a Potassium-sparing diuretic on ventricular myocardial remodeling and on arrhythmia burden in patients with ARVD. The trial is a double-blind parallel multicenter prospective randomized phase II drug study. Patients will be randomized in the two groups: spironolactone or placebo. 13 centers in France will enroll the 120 patients (60 per group). Patients will be followed for 3 years (6 months, 1 year and 3 years) with all examinations (ECG, HA ECG, 24-hour Holter, trans-thoraciqc echocardiography (TTE), biological analyses) according to standard of care. A decrease in right and/or left ventricular deterioration and in arrhythmia burden are expected in ARVD patients treated with spironolactone. This reduction will improve the quality of life of patients and will reduce the number of hospitalizations and the risk of terminal heart failure.
Official title: Blockade of the Renin-angiotensin-aldosterone System in Patients With ARVD: a Double-blind Multicentre Prospective Randomized Study.
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
120
Start Date
2024-12-20
Completion Date
2029-12
Last Updated
2026-02-09
Healthy Volunteers
No
Interventions
Spironolactone
The doses used in the study are the doses used in standard clinical practice. Initial dose is 25 mg/day until study end . The duration of treatment for each patient is 12 months.
Placebo
Placebo will be taken once a day at the same time of day. The duration of treatment for each patient is 12 months.
Locations (13)
CHU Amiens Picardie
Amiens, France
Hôpital Cardiologique Louis Pradel
Bron, France
Hôpital Gabriel Montpied
Clermont-Ferrand, France
CHU Dijon
Dijon, France
Hôpital Michallon
Grenoble, France
Hôpital de la Timone
Marseille, France
Hôpital Arnaud de Villeneuve
Montpellier, France
Hôpital Laennec
Nantes, France
Groupe Hospitalo Universitaire Caremeau
Nîmes, France
Hôpital Pitié Salpetrière
Paris, France
Hôpital de Haut-Lévêque
Pessac, France
Nouvel Hôpital Civil
Strasbourg, France
Hôpital Rangueil
Toulouse, France