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Clinical Trial Summary

Prospective, multicenter, randomized, placebo-controlled, double-blind clinical trial to evaluate safety and efficacy of candesartan in the prevention of the development of Dilated Cardiomyopathy (DCM) in genetic carriers of a DCM-causing variant without disease expression (asymptomatic)


Clinical Trial Description

Prospective, multicenter, randomized, placebo-controlled, double-blind clinical trial to evaluate safety and efficacy of early administration of candesartan in the prevention of the development of Dilated Cardiomyopathy (DCM) in genetic carriers of a DCM-causing variant without disease expression (asymptomatic). Randomization will be 1:1 and patients are allocated to candesartan or matching placebo. Patients will be followed for a 3 years period and efficacy will be demonstrated if candesartan (compared to placebo) prevents either a significant Left ventricular ejection fraction (LVEF) decline of ≥10%, or a ventricular dilatation (left ventricular end-diastolic volume, LVEDV) increase of ≥10% within a 3-years period of follow-up ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05321875
Study type Interventional
Source Puerta de Hierro University Hospital
Contact Cristina Avendaño-Solá, MD, PhD
Phone +34 91 1916479
Email cavendano@salud.madrid.org
Status Recruiting
Phase Phase 3
Start date June 2, 2022
Completion date June 2, 2026

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