A Comparison Of The Effects Of Added Metformin (Versus No Added Metformin) On Psychopathology, Lipids, And Measures of Inflammation During The Initiation Or Re-Institution Of Treatment With Clozapine In Patients With Schizophrenia Or Schizoaffective Disorder
Overview
- Phase
- Phase 4
- Intervention
- Metformin
- Conditions
- Schizophrenia
- Sponsor
- Duke University
- Enrollment
- 34
- Primary Endpoint
- Change in Weight
- Status
- Terminated
- Last Updated
- 2 years ago
Overview
Brief Summary
One purpose of this study is to test whether adding metformin will limit some of the unwanted effects of clozapine, compared to not adding metformin. Metformin is a medication that is approved by the United States Food and Drug Administration (FDA) for the treatment of type-2 diabetes. Studies have found that people with type-2 diabetes often lose some weight when they take metformin, however the FDA has not approved metformin for weight loss, so for this study the use of metformin is investigational. This study will test whether metformin can help people with schizophrenia or schizoaffective disorders lose weight.
Another purpose of this study is to test whether adding fish oil will improve the benefit of clozapine and/or limit some of the unwanted effects of clozapine, compared to not adding fish oil. Fish oil is a medication used to reduce levels of some fats (triglycerides) in blood. Some studies have found that adding fish oil reduces psychosis (voices, suspiciousness). However the FDA has not approved fish oil for reducing psychosis, so for this study the use of fish oil is investigational. This study will test whether fish oil can help people with schizophrenia or schizoaffective disorders have less psychosis. Fish oil is not an antipsychotic medication.
Investigators
Eligibility Criteria
Inclusion Criteria
- •male or female patients with clinical diagnoses of schizophrenia or schizo-affective disorder
- •between 18 and 60 years of age
- •patients whose treating clinicians have recommended treatment with clozapine (and the patients have agreed and provided signed informed consent for treatment with clozapine)
Exclusion Criteria
- •patients who have contraindications to metformin use, such as:
- •a diagnosis of congestive heart failure
- •renal impairment (serum creatinine \> 1.5 in males; \> 1.4 in females)
- •hepatic disease (AST or ALT \> 2.0 times upper limit of normal (ULN)
- •positive hepatitis B surface antigen or hepatitis C antibody
- •total bilirubin\>1.2x ULN; majority conjugated
- •metabolic acidosis (serum CO2 \< lower limit of normal),
- •known hypersensitivity to metformin,
- •recent (in the past 30 days) or scheduled radiological studies involving iodinated contrast material
- •alcohol abuse/dependence within the past month
Arms & Interventions
Metformin
Subjects will continue to take the clozapine prescribed as standard of care. Subjects assigned to added metformin will receive metformin 250 mg BID days 1-3, 500 mg BID days 4-7, and 1000 mg BID days 8-28 with breakfast and supper. Patients unable to tolerate a dose escalation will have the metformin dose reduced to the previously tolerated lower dose.
Intervention: Metformin
Fish Oil
Subjects will continue to take the clozapine prescribed as standard of care. Subjects assigned to added fish oil will receive OmegaBrite 500 mg gel cap BID days 1-7, and 1000 mg BID days 8-28 with breakfast and supper. Patients unable to tolerate the dose escalation to 1000 mg BID will have the fish oil dose reduce to 500 mg BID.
Intervention: Fish Oil
Metformin and Fish Oil
Subjects will continue to take the clozapine prescribed as standard of care. Subjects will receive Metformin and Fish Oil as part of the study.
Intervention: Metformin
Metformin and Fish Oil
Subjects will continue to take the clozapine prescribed as standard of care. Subjects will receive Metformin and Fish Oil as part of the study.
Intervention: Fish Oil
Outcomes
Primary Outcomes
Change in Weight
Time Frame: baseline, 2 weeks, 4 weeks
Secondary Outcomes
- Changes in Fasting Levels of Non-HDL Cholesterol and Triglycerides(baseline, 2 weeks, 4 weeks)
- Changes in C-reactive Protein and Sedimentation Rates(baseline, 2 weeks, 4 weeks)
- Changes in Mole Percentages of Omega-3 PUFAs in Fasting Serum and RBC Membranes(baseline, 2 weeks, 4 weeks)
- Changes in Total Scores on the 4 Positive Brief Psychiatric Rating Scale (BPRS) Items(baseline, 2 weeks, 4 weeks)