Efficacy of Quetiapine in the Treatment of Patients With Schizophrenia and a Comorbid Substance Use Disorder

PHASE4CompletedINTERVENTIONAL
Enrollment

23

Participants

Timeline

Start Date

March 31, 2004

Primary Completion Date

September 30, 2006

Study Completion Date

October 31, 2008

Conditions
SchizophreniaSchizoaffective DisorderPsychotic DisorderSubstance AbuseAlcohol Abuse
Interventions
DRUG

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.

Trial Locations (4)

30912

Medical College of Georgia, Augusta

03756

Dartmouth-Hitchcock Medical Center, Lebanon

03766

West Central Behavioral Health, Lebanon

03101

Mental Health Center of Greater Manchester, Manchester

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Augusta University

OTHER

collaborator

AstraZeneca

INDUSTRY

lead

Dartmouth-Hitchcock Medical Center

OTHER

NCT00156715 - Efficacy of Quetiapine in the Treatment of Patients With Schizophrenia and a Comorbid Substance Use Disorder | Biotech Hunter | Biotech Hunter