An 8-week study to examine safety and efficacy of levetiracetam in patients with neuroleptic-induced tardive dyskinesia
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Masking
DOUBLE
Enrollment
70
Unnamed facility
Antwerp, Belgium
Unnamed facility
Bourgois, Belgium
Unnamed facility
Gonce, Belgium
Unnamed facility
Hulselmans, Belgium
Unnamed facility
Liège, Belgium
Reduction in neuroleptic-induced tardive dyskinesia over an 8 week treatment period
Neuroleptic-induced akathisia and other extrapyramidal symptoms ,
Effect on the primary psychiatric disorder
Safety
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Unnamed facility
Roeselare, Belgium
Unnamed facility
Haralanov, Bulgaria