The purpose of this clinical trial is to test whether or not the medication amantadine is effective in reducing behavioral disturbances in patients with frontotemporal dementia.
Behavioral disturbances are a major cause of morbidity in frontotemporal dementia (FTD), yet little is known about the effectiveness of medications to treat these disturbances. Preliminary data suggests that the dopaminergic agent amantadine may reduce these disturbances. This 6-week, prospective, randomized, placebo-controlled trial will compare amantadine to placebo to assess its effectiveness in reducing behavioral symptoms.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Johns Hopkins University School of Medicine, Outpatient General Clinical Research Center
Baltimore, Maryland, United States
Frontal Behavioral Inventory, disinhibition subscale
Time frame: 6 weeks
Frontal Behavior Inventory, total score
Time frame: 6 weeks
Neuropsychiatric Inventory
Time frame: 6 weeks
Apathy Evaluation Scale
Time frame: 6 weeks
Cognitive measures - Mini Mental State Exam (MMSE), Trails Making Test A&B (Trails A&B), Verbal fluency, and Stroop test
Time frame: 6 weeks
Activities of Daily Living (ADL) and Instrumental Activities of Daily Living (IADL) measures
Time frame: 6 weeks
Zarit Burden Interview
Time frame: 6 weeks
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