Stopped: No participants enrolled
The intent of this clinical study is to answer the questions: 1. Is the proposed treatment safe 2. Is treatment effective in improving the disease pathology of patients with diffuse brain lesions and clinical outcomes.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Improvement in standardized Gross Motor Function Measure evaluation compared to baseline
Timeframe: 3 months
Number of participants with adverse events
Timeframe: up to 6 months
Improved cognitive function as measured by the mini mental state exam
Timeframe: 3 months
Improvement in standardized Gross Motor Function Measure evaluation compared to baseline
Timeframe: 6 months
Improved cognitive function as measured by the mini mental state exam compared to baseline
Timeframe: 6 months
Reduced depressive symptoms measured by the Beck Depression Inventory compared to baseline
Timeframe: 3 months
Reduced depressive symptoms measured by the Beck Depression Inventory compared to baseline
Timeframe: 6 months