Ignite Creation Date:
2024-05-05 @ 12:03 PM
Last Modification Date:
2024-10-26 @ 9:19 AM
Study NCT ID:
NCT00221832
Status:
UNKNOWN
Last Update Posted:
2010-01-13
First Post:
2005-09-14
Brief Title:
Molecular Genetic Screening and Identification of Congenital Arrhythmogenic Diseases
Sponsor:
Organization:
Heidelberg University
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:
no biospecimens are to be retained
Enrollment Count:
300
Enrollment Type:
ESTIMATED
Design Primary Purpose:
Design Masking:
Phases:
Observational Models:
| Name |
|---|
| Family-Based |
Time Perspective List:
Clinical Trial Statuses
| Name |
|---|
| 1466 |
Who Masked List: