"Detection and Follow-up of Coronary Lesions in HeFH (DESTINY-FH Study)"

Recruiting N/A Interventional Study
Heterozygous Familial Hypercholesterolemia (HeFH)
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
30 – 60
Sex
Any
Study type
Interventional
Purpose
Prevention
Participants needed
300 (estimated)
Sponsor
Assistance Publique - Hôpitaux de Paris · Other
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About This Trial
This multicenter, non-randomized interventional study aims to assess coronary artery disease progression over 5 years in patients with genetically confirmed heterozygous familial hypercholesterolemia (HeFH), using coronary computed tomography angiography (CCTA). The primary endpoint is the visual evaluation of coronary stenosis using CAD-RADS v2.0, identifying changes between baseline (2018-2022)…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Patients with heterozygous familial hypercholesterolemia 2. Aged 30 to 60 years. 3. Patients who underwent a CAC score and a coronary CT angiogram at least 5 years ago, exclusively at the same imaging center (ICT de la Pitié Salpetrière). 4. Patient asymptomatic for exertiona…
Contacts

Antonio GALLO, MD, PhD

33(0)1 42 17 57 74

antonio.gallo@aphp.fr

CONTACT

Franck BOCCARA, MD, PhD

33(0)1 49 28 24 49

franck.boccara@aphp.fr

CONTACT