Screening of Fabry Disease in Patients With Left Ventricular Hypertrophy Detected in Echocardiography
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|ClinicalTrials.gov Identifier: NCT02221141|
Recruitment Status : Unknown
Verified January 2018 by Laurence Gabriel, Centre Hospitalier Universitaire Dinant Godinne - UCL Namur.
Recruitment status was: Recruiting
First Posted : August 20, 2014
Last Update Posted : February 1, 2018
The purpose of this study is to determine the prevalence in Belgium of Fabry disease in patients with unexplained hypertrophic cardiomyopathy measured by echocardiography and to determine in Fabry patients which was the most frequently initial symptom.
Actually the early diagnosis is important because a treatment exists that can prevent future complications.
|Condition or disease|
|Left Ventricular Hypertrophy|
|Study Type :||Observational|
|Estimated Enrollment :||300 participants|
|Study Start Date :||December 2013|
|Estimated Primary Completion Date :||December 2018|
|Estimated Study Completion Date :||December 2018|
- Percentage of patients with left ventricular hypertrophy who have Fabry Disease mutation [ Time Frame: 1 day ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02221141
|Contact: Laurence Gabriel||+32 81 42 21 11 ext email@example.com|
|Contact: Karine Jourdan||+32 81 42 21 11 ext firstname.lastname@example.org|
|Yvoir, Belgium, 5530|
|Principal Investigator: Laurence Gabriel|