23
Participants
Start Date
March 31, 2004
Primary Completion Date
September 30, 2006
Study Completion Date
October 31, 2008
Quetiapine
After patients provided informed consent and completed baseline measures, quetiapine was initiated in all participants and titrated up to a target dose of 600 mg (in divided daily doses) over two weeks as the previous antipsychotic medication was slowly tapered and discontinued. Participants met with study physicians weekly to assess tolerability and response to the medication. Concomitant medications were held constant. After the initial titration period, quetiapine was dosed in a flexible manner up to 800 mg /day, with dose adjustments based on symptomatic response and side effects.
Medical College of Georgia, Augusta
Dartmouth-Hitchcock Medical Center, Lebanon
West Central Behavioral Health, Lebanon
Mental Health Center of Greater Manchester, Manchester
Collaborators (1)
Augusta University
OTHER
AstraZeneca
INDUSTRY
Dartmouth-Hitchcock Medical Center
OTHER