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Effects of Pravastatin on Cholesterol, Inflammation and Cognition in Schizophrenia - NCT01082588-02114(Clinical Trial 567173)



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City:  Boston
State:  
MA
Zip Code: 02114
Conditions: Schizophrenia - Schizoaffective Disorders - Schizophreniform Disorders
Purpose: This study involves people with schizophrenia or schizoaffective disorder, who are currently taking antipsychotic medications. Some antipsychotic medications may cause an increase in cholesterol levels, which may lead to inflammation in the body. Inflammation poses a risk in developing heart disease, diabetes and problems with brain function. The purpose of this study is to see if pravastatin can: - Lower cholesterol - Decrease inflammation - Improve cognition in patients with schizophrenia
Study summary: This study is a 12-week randomized, double-blind, placebo-controlled pilot study of pravastatin 40mg a day, administered for 12 consecutive weeks to subjects with schizophrenia to examine pravastatin's effects on lowering cholesterol levels and inflammatory markers, and improving cognition. The study will be conducted at the Freedom Trail Clinic and will use the Massachusetts General Hospital Clinical Research Center. The innovative approach of using pravastatin to not only decrease cholesterol levels, but to decrease inflammation and improve cognition in patients with schizophrenia is promising and may lead to a different approach to treatment in this population.
Criteria: Inclusion Criteria: - Male or female - Age 18-68 years - Diagnosis of schizophrenia, any subtype, schizoaffective disorder, any subtype or schizophreniform disorder - Well established compliance with outpatient medications including their antipsychotic medication Exclusion Criteria: - Inability to provide informed consent - Current substance and alcohol abuse - Significant medical illness, including congestive heart failure, severe cardiovascular disease, renal disease (serum creatinine > 1.5), severe hepatic impairment or active liver disease, anemia (hemoglobin <11.0 gm/dL), history of severe head injury, and not treated muscle disease. - Psychiatrically unstable - Women of child bearing potential who are pregnant, breastfeeding, or who are unwilling or unable to use an effective form of birth control during the entire study - Subjects treated with anti-inflammatory drugs (including daily aspirin and ibuprofen), thiazide diuretics; agents that induce weight loss, and St. John's Wort will be excluded from the study - Current history of untreated thyroid disease - Current treatment with insulin - Subjects being treated with drugs such as: colchicine, azole antifungals (fluconazole, ketoconazole, itraconazole); macrolide antibiotics (clarithromycin, erythromycin); HIV protease inhibitors (ritonavir, indinavir, saquinavir, nelfinavir) that inhibit the CYP 450 3A liver enzyme - Known hypersensitivity to pravastatin or any of its components
Study is available at: Freedom Trail Clinic
Boston, MA 02114
United States

Primary Contact:
Sarah Cleary
Email: smcleary@partners.org
Phone: 617-912-7882
If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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Data Source: ClinicalTrials.gov
Date Processed: March 23, 2011
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