This is a preliminary study to determine the safety and efficacy of intravenous immune globulin in treating Spinocerebellar Ataxia. The investigators aim to assess changes in clinical measures of disease severity before and after treatment.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
5
Intravenous Immune Globulin
University of South Florida
Tampa, Florida, United States
Scale for the Assessment and Rating of Ataxia
Time frame: participants will be followed for approximately 4 months
Timed 25 foot walk
Time frame: participants will be followed for approximately 4 months
Clinical Global impression
Time frame: participants will be followed for approximately 4 months
Biodex Balance SD
Time frame: participants will be followed for approximately 4 months
Gait Rite Mat
Time frame: participants will be followed for approximately 4 months
Berg balance scale
Time frame: participants will be followed for approximately 4 months
Complete Metabolic Panel
Time frame: participants will be followed for approximately 4 months
Complete Blood Count
Time frame: participants will be followed for approximately 4 months
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