Clinical and Molecular Correlations in Spinocerebellar Ataxia Type 10 (SCA10)

Completed

Conditions studied: Hereditary Ataxia

In brief

OBJECTIVES: I. Clinically evaluate members from families with a dominantly inherited ataxia and collect blood, skin and muscle samples for detailed molecular studies. II. Perform detailed clinical evaluations on patients with recessively inherited ataxias.

Key facts

Study ID

NCT00004306

Run by

Office of Rare Diseases (ORD)

People needed

18

Starts

1999-11-01

Expected to finish

2009-03-01

Last updated by the study team

2012-03-06

Who can join

Age: 3 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects who have the diagnosis of SCA10 and their immediate relatives.

You may not qualify if…

• Children under 3 years of age, pregnant women, prisoners, mentally incapacitated subjects, and subjects who do not give consent.

Where it is running

• University of Texas Medical Branch at Galveston — Galveston, Texas, United States

Full record on ClinicalTrials.gov

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