Valproate in Late Life Schizophrenia

PHASE4CompletedINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

November 30, 2004

Primary Completion Date

November 30, 2006

Study Completion Date

November 30, 2006

Conditions
Schizophrenia
Interventions
DRUG

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.

Trial Locations (1)

44106

University Hospitals of Cleveland, Cleveland

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Abbott

INDUSTRY

lead

University Hospitals Cleveland Medical Center

OTHER