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French Registry: Late Gadolinium Enhancement in Hypertrophic Cardiomyopathy

Retrospective French Registry of Cardiovascular Magnetic Resonance Late Gadolinium Enhancement in Patients With Hypertrophic Cardiomyopathy

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07428031
Acronym
HCM-LGE
Enrollment
5000
Registered
2026-02-23
Start date
2026-03-01
Completion date
2036-03-01
Last updated
2026-02-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiomyopathy, Hypertrophic Cardiomyopathies

Keywords

Cardiac Magnetic Resonance, Cardiomyopathy

Brief summary

This study aims to create a registry of patients with hypertrophic cardiomyopathy, a condition characterized by excessive thickening of the heart muscle. This disease can sometimes lead to serious complications. Currently, the prognosis of these patients is mainly determined by clinical and echocardiographic parameters. Detection of myocardial fibrosis using cardiac MRI enables better risk stratification for these patients.

Interventions

None listed

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Age ≥ 18 years 2. Ability to provide informed consent 3. HCM diagnosis referred for CMR assessment.

Exclusion criteria

1. Patients unable to provide informed consent, 2. Patients with a history of ischemic cardiomyopathy or myocarditis.

Design outcomes

Primary

MeasureTime frameDescription
To build a score using the "LGE granularity" concept for all-cause mortality prediction in HCM patients.From Baseline to 5 yearsAll-cause mortality using the electronic French National Registry of Death (Institut National de la Statistique et des Etudes Economiques, INSEE registry).

Contacts

CONTACTThéo PEZEL, Dr
theo.pezel@aphp.fr+33 6 68 72 24 89

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026