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RECRUITING
NCT03593317
PHASE2

Blockade of the Renin-angiotensin-aldosterone System in Patients With ARVD

Sponsor: Hospices Civils de Lyon

View on ClinicalTrials.gov

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

DRUG

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.

DRUG

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