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French Hypertrophic Cardiomyopathy Observatory

French Hypertrophic Cardiomyopathy Observatory

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01091480
Acronym
REMY
Enrollment
600
Registered
2010-03-24
Start date
2010-01-31
Completion date
2028-12-31
Last updated
2022-09-21

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

Conditions

Hypertrophic Cardiomyopathy

Keywords

Hypertrophic cardiomyopathy, Observatory, LVH

Brief summary

Hypertrophic cardiomyopathy (Hypertrophic CardioMyopathy=HCM) remains a poorly understood disease with an assumption insufficiently codified. There is no data available in France on the profile of patients, diagnostic methods and assessment and therapeutic use. The purpose of this study is to establish a monitoring of patients with HCM (sarcomere of origin or not) in France (diagnosis, treatment)

Detailed description

This both retrospective and prospective study is proposed to cardiology services 50 hospitals in France. A cardiologist referral is designated for each facility. The following data will be collected by the physician during the initial hospitalization * Demographics * Geographic origin of patient * Clinical data: criteria for inclusion and non-inclusion data HCM general, Doppler ultrasound, personal history, family history * Reviews made: non-organic, biological * Family Survey, * Treatments: Medical, Electrical, invasive * Data from hospital The follow-up to 18 months, 3 years and 5 years will be conducted by clinical-research-technicians of the French Society of Cardiology, an application will be made to municipalities of birth and mail a letter to physicians and patients. The following data will be collected: * Vital status * Data from hospital * Reviews made: non-organic, biological * Treatments: Medical, Electrical, invasive

Interventions

None listed

Sponsors

French Cardiology Society
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

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

Inclusion criteria

* Age ≥ 15 years old * Patient with HCM defined by an ultrasound thickness of the left ventricle ≥ 13 mm if familial or ≥ 15 mm if sporadic

Exclusion criteria

* Expressed refusal to participate in the study * Significant aortic stenosis (\<1 cm ²)

Design outcomes

Primary

MeasureTime frame
Event-free survival3 years

Secondary

MeasureTime frameDescription
Diagnostic methods0 dayDefine the profile of patients with HCM in France, diagnostic methods, evaluation (diagnostic investigation and family) and therapeutic. Who are the patients CMH France? (rules discovery, clinical presentation) and how are assumed the HCM in France? (examinations, hospitalizations, treatments, procedures for the family survey).

Countries

France

Contacts

Primary ContactAlbert Hagege
albert.hagege@egp.ap-hop-paris.fr33(0)156092897

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026