20
Participants
Start Date
November 30, 2004
Primary Completion Date
November 30, 2006
Study Completion Date
November 30, 2006
Valproate
Enrolled individuals received adjunctive, open-label valproate semisodium, initially started as valproate semisodium delayed -release 250 mg at bedtime for two weeks, then changed to valproate semisodium extended- release 500 mg at bedtime. Medication was administered on an outpatient/ambulatory basis, and adjusted as tolerated to target serum levels of 50-100 µg/mL. In cases where sedation or other side effects occurred, dosage was reduced. Valproate semisodium was prescribed in a single dose at bedtime.
University Hospitals of Cleveland, Cleveland
Collaborators (1)
Abbott
INDUSTRY
University Hospitals Cleveland Medical Center
OTHER