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Belgian Screening Project for the Detection of Anderson-Fabry Disease in Hypertrophic Cardiomyopathy

G

Ghent University Hospital (UZ)

Status

Completed

Conditions

Left Ventricular Hypertrophy

Treatments

Other: blood sampling

Study type

Observational

Funder types

Other

Identifiers

NCT01198899
2009/035

Details and patient eligibility

About

The purpose of this study is to determine the prevalence of Fabry mutations in patients with left ventricular hypertrophy (moderate to severe), as measured by echocardiography.This study is a screening study

Enrollment

540 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • All patients over 18 years undergoing a routine echocardiography in the participating hospitals
  • Both genders will be considered.
  • Patients can be included if on 2D echocardiography the maximal septal wall thickness > 13 mm and/or the posterior wall thickness > 13 mm. The limit for inclusion is kept relatively low to detect early forms of Fabry cardiomyopathy.

Trial design

540 participants in 1 patient group

left ventricular hypertrophy
Description:
Patients with left ventricular hypertrophy will be used.
Treatment:
Other: blood sampling

Trial contacts and locations

9

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Data sourced from clinicaltrials.gov

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