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Registry and prevalence of gene mutation in Korean patients with familial hypertrophic cardiomyopathy

Registry and prevalence of gene mutation in Korean patients with familial hypertrophic cardiomyopathy

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0000777
Enrollment
250
Registered
2013-06-25
Start date
2013-03-21
Completion date
Unknown
Last updated
2019-03-11

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

Conditions

None listed

Interventions

None listed

Sponsors

Korea Centers for Disease Control and Prevention
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed as hypertrophic cardiomyopathy 2. Family members of diagnosed patients 3. In cases of juvenile, above age-13(yrs) Patients (male or female) who is diagnosed as hypertrophic cardiomyopathy following the guidlines, were to be asked and voluntarily participated with signing the consent to participate in research - Guidelines a. (Adults) Without the effect of hypertrophy-causing cardiac risks (fabry disease, danon disease, glycogen storage disease, etc.), maximal wall thickness (MWT) are increased more than 15mm in left ventricle with the echocardiography result. b. (in juveniles(age-13 and above)) MWT are relatively increased as adults with regard to body surface area, and not dilated.

Exclusion criteria

Exclusion criteria: - Patients and family members who disagreed with the participation of research

Design outcomes

Primary

MeasureTime frame
Types of Cardiomyopathy (CMP)

Secondary

MeasureTime frame
Patient's pedigree infomation

Countries

Korea, Republic of

Contacts

Public ContactSeok-Min Kang

Yonsei University Health System, Severance Hospital

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026