Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
Register:
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ClinicalTrials.gov |
Last refreshed on:
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19 February 2015 |
Main ID: |
NCT01198899 |
Date of registration:
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31/08/2010 |
Prospective Registration:
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No |
Primary sponsor: |
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Public title:
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Belgian Screening Project for the Detection of Anderson-Fabry Disease in Hypertrophic Cardiomyopathy
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Scientific title:
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Belgian Screening Project for the Detection of Anderson-Fabry Disease in Hypertrophic Cardiomyopathy |
Date of first enrolment:
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July 2009 |
Target sample size:
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540 |
Recruitment status: |
Completed |
URL:
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http://clinicaltrials.gov/show/NCT01198899 |
Study type:
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Observational |
Study design:
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Observational Model: Cohort, Time Perspective: Prospective
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Phase:
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N/A
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Countries of recruitment
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Belgium
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Contacts
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Name:
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Raymond Vanholder, MD, PhD |
Address:
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Telephone:
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Email:
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Affiliation:
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University Hospital Ghent, Belgium |
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Key inclusion & exclusion criteria
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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.
Age minimum:
18 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Left Ventricular Hypertrophy
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Intervention(s)
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Other: blood sampling
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Primary Outcome(s)
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Determination of the prevalence of Fabry mutations in patients with left ventricular hypertrophy (moderate to severe), as measured by echocardiography
[Time Frame: At baseline T0]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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