Schizophrenia Clinical Trial
Official title:
Omega-3 Fatty Acids (Lovaza) for Second Generation Antipsychotic-Associated Hypertriglyceridemia
Verified date | April 2014 |
Source | Massachusetts General Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Interventional |
This is an open-label pilot study of omega-3 fatty acids (Lovaza) for hypertriglyceridemia in subjects who have been on an atypical (second-generation) antipsychotic medication. The investigators hypotheses are that patients who receive Lovaza will experience a significant decrease in triglycerides from baseline. Secondary hypotheses include: Patients will experience a significant decrease in total cholesterol, and Lovaza will be well tolerated.
Status | Completed |
Enrollment | 40 |
Est. completion date | March 2013 |
Est. primary completion date | March 2013 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 75 Years |
Eligibility |
Inclusion Criteria: 1. Female or male patients, 18-75 years of age. 2. Serum triglycerides >200 mg/dl or high cholesterol >250 mg/dl 3. Current use of an atypical (second-generation) antipsychotic medication - including clozapine (Clozaril), olanzapine (Zyprexa), risperidone (Risperdal), aripiprazole (Abilify), ziprasidone (Geodon), quetiapine (Seroquel), paliperidone (Invega) - for at least three months Exclusion Criteria: 1. Current use of triglyceride or cholesterol-lowering medication other than a statin 2. Current use of omega-3 fatty acid supplement 3. Intake of fish more than twice per week 4. Currently pregnant, or breastfeeding 5. Known hypersensitivity or allergy to omega-3 fatty acids (or any fish allergies) 6. Current use of anticoagulant medication, except for 1 baby aspirin/day - 81mg (coumadin, heparin, Plavix. etc). 7. Consumption of alcohol greater than two drinks per day or active substance abuse 8. Any medical condition that would make participation in the study unsafe, as determined by investigator |
Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | Massachusetts General Hospital | Boston | Massachusetts |
Lead Sponsor | Collaborator |
---|---|
Massachusetts General Hospital | GlaxoSmithKline |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | decrease in triglycerides from baseline | 16 weeks | No | |
Secondary | decrease in total cholesterol and tolerability | 16 weeks | No |
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