Ignite Creation Date:
2024-05-05 @ 5:14 PM
Last Modification Date:
2024-10-26 @ 9:29 AM
Study NCT ID:
NCT00414583
Status:
COMPLETED
Last Update Posted:
2021-04-09
First Post:
2006-12-19
Brief Title:
Stroke in Young Fabry Patients sifap1 Frequency of Fabry Disease in Young Stroke Patients
Sponsor:
Organization:
CENTOGENE GmbH Rostock
Study Design
Study Type:
OBSERVATIONAL
Expanded Access Type Individual:
None
Expanded Access Type Intermediate:
None
Expanded Access Type Treatment:
None
Patient Registry:
None
Target Duration:
None
Design Allocation:
Design Intervention Model:
Design Intervention Model Description:
Design Masking Description:
Bio Spec Retention:
SAMPLES_WITH_DNA
Bio Spec Description:
Fabry diagnostic will be done centrally blood samples will be retained for analysis of a-galactosidase in blood to diagnose an a-galactosidase deficit in females direct analysis of the gene has to be done since due to the Lyonisation effect a-galactosidase activity might be normal in blood although the patient might suffer from Fabry disease
Enrollment Count:
5000
Enrollment Type:
ACTUAL
Design Primary Purpose:
Design Masking:
Phases:
Observational Models:
| Name |
|---|
| Cohort |
Time Perspective List:
Clinical Trial Statuses
| Name |
|---|
| 2800 |
Who Masked List: