Viewing StudyNCT00136630



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Last Modification Date: 2024-10-26 @ 9:13 AM
Study NCT ID: NCT00136630
Status: COMPLETED
Last Update Posted: 2021-08-25
First Post: 2005-08-25

Brief Title: Natural History Genetic Bases and Phenotype-genotype Correlations in Autosomal Dominant Spinocerebellar Degenerations
Sponsor:
Organization: Institut National de la Santé Et de la Recherche Médicale France

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: None
Bio Spec Description: None
Enrollment Count: 175
Enrollment Type: ACTUAL
Design Primary Purpose:
Design Masking:
Phases:
Observational Models:
Name
Family-Based
Time Perspective List:

Clinical Trial Statuses

Name
697
Who Masked List: