Use of Galantamine and CDP-choline (Citicoline) to Treat Adults With Schizophrenia

PHASE2CompletedINTERVENTIONAL
Enrollment

43

Participants

Timeline

Start Date

November 30, 2007

Primary Completion Date

March 31, 2011

Study Completion Date

March 31, 2011

Conditions
Schizophrenia
Interventions
DRUG

Galantamine

Galantamine will be titrated to 24 mg/day over 2 weeks. Participants will receive 8 mg/day in two divided doses for 1 week, 16 mg/day in two divided doses for 1 week, and 24 mg/day in two divided doses beginning in Week 3. They will be maintained on 24 mg/day for the remainder of the study.

DRUG

CDP-choline

CDP-choline will serve as the dietary source of choline. CDP-choline will be titrated to 2000 mg/day over 1 week. Subjects will receive 500 mg/day for 3 days; Thereafter, the dose of CDP-choline will be increased to 1,000 mg/day in two divided doses for 4 days. At the beginning of Week 2, participants will receive the maximum fixed dose of 2000 mg/day in two divided doses, which will be held constant through the end of Week 16.

DRUG

Placebo

The schedule of dose titration of placebo galantamine and placebo CDP-choline will follow the schedule of active medication condition using matching placebos for each agent.

DRUG

risperidone, olanzapine, quetiapine, ziprasidone, and/or aripiprazole

All participants will continue to take their regular regimen of risperidone, olanzapine, quetiapine, ziprasidone, and/or aripiprazole throughout the trial in addition to their assigned treatment.

Trial Locations (1)

20422

Washington Veterans Affairs Medical Center, Washington D.C.

All Listed Sponsors
collaborator

National Institute of Mental Health (NIMH)

NIH

collaborator

Washington D.C. Veterans Affairs Medical Center

FED

lead

Georgetown University

OTHER

NCT00509067 - Use of Galantamine and CDP-choline (Citicoline) to Treat Adults With Schizophrenia | Biotech Hunter | Biotech Hunter