The purpose of the study is to determine if lipoic acid can protect the brain and slow disability in secondary progressive multiple sclerosis.
There are no approved medications that are neuroprotective or able to slow disability accumulation in secondary progressive multiple sclerosis (SPMS). This two-year study will determine if daily oral intake of lipoic acid, a natural supplement, will prove superior to placebo in reducing injury to the brain and reducing disability progression in SPMS. Neuroprotection will be measured by the extent of brain volume loss seen on MRI, and disability will be measured by neurological status and quality of life.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
54
1200 mg taken by mouth daily starting on day one of the study and ending on the last day of study participation.
The placebo comparator will be taken by mouth daily starting on day one of the study and ending on the last day of study participation
VA Portland Health Care System, Portland, OR
Portland, Oregon, United States
Brain Atrophy by MRI
Time frame: % change brain volume from baseline to year 2
Disability Measures: Mobility
Time frame: Change in Timed 25 Foot Walk from baseline to year 2
Safety Measure: Adverse Events
Time frame: adverse events recorded from baseline to year 2
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