RecruitingPhase 2NCT03593317

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

Blockade of the Renin-angiotensin-aldosterone System in Patients With ARVD: a Double-blind Multicentre Prospective Randomized Study.


Sponsor

Hospices Civils de Lyon

Enrollment

120 participants

Start Date

Dec 20, 2024

Study Type

INTERVENTIONAL

Conditions

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.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This trial is studying whether blocking a hormone system in the body (called the renin-angiotensin-aldosterone system) can help people with a hereditary heart condition called ARVD (arrhythmogenic right ventricular dysplasia), which affects the electrical and structural function of the heart. **You may be eligible if...** - You are over 18 years old - You have been diagnosed with ARVD based on established medical criteria - Your heart's pumping function (specifically the left side) is above 40% - You have health insurance - You agree to use effective contraception if you are of childbearing age **You may NOT be eligible if...** - You are pregnant, breastfeeding, or planning to become pregnant - You do not have health insurance - You have severe right-sided heart failure - You are under judicial protection - Your left heart pumping function is below 40% Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGSpironolactone

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.

DRUGPlacebo

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

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NCT03593317


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