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Sponsors and Collaborators: |
Weill Medical College of Cornell University Stanley Medical Research Institute |
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Information provided by: | Weill Medical College of Cornell University |
ClinicalTrials.gov Identifier: | NCT00615511 |
Four-month trial of pregnenolone or placebo, as an additional medication, to treat negative symptoms and cognitive decline in schizophrenia. After four months the scores on the negative symptom scale should be lower and the scores on the cognitive tests should be higher than they were at study entry, compared with people who do not take any additional medication.
Condition | Intervention | Phase |
---|---|---|
Schizophrenia Schizoaffective Disorder |
Dietary Supplement: pregnenolone |
Phase II |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double Blind (Subject, Outcomes Assessor), Placebo Control, Parallel Assignment, Efficacy Study |
Official Title: | Efficacy of Pregnenolone in Patients With Schizophrenia |
Estimated Enrollment: | 100 |
Study Start Date: | May 2007 |
Estimated Study Completion Date: | November 2009 |
Estimated Primary Completion Date: | November 2009 (Final data collection date for primary outcome measure) |
Arms | Assigned Interventions |
---|---|
1: Placebo Comparator |
Dietary Supplement: pregnenolone
Titration over first four weeks up to 500mg per day, in the form of five small pills to be taken by mouth each morning and evening, with or without food.
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2: Experimental
High dose dietary supplement intervention
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Dietary Supplement: pregnenolone
Titration over first four weeks up to 500mg per day, in the form of five small pills to be taken by mouth each morning and evening, with or without food.
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Pregnenolone is a steroid health supplement which is readily available in health food stores. We are using it in this study at higher doses than you would normally take as a health supplement because preliminary studies have indicated that negative symptoms improve and certain aspects of cognition improve at these doses. We do not require you to stop your existing treatment in order to enter the study. After four months we will test your symptoms and cognition and ask if you would like to continue taking pregnenolone, at no cost, in a follow-up study designed to determine the long-term costs and benefits of taking pregnenolone.
Ages Eligible for Study: | 18 Years to 65 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contact: Adam J Savitz, MD, PhD | 914 997 4394 | ads9002@med.cornell.edu |
Contact: Judith M English, MA | 914 682 6974 | jme2003@med.cornell.edu |
United States, New York | |
Weill Medical College of Cornell University | Recruiting |
White Plains, New York, United States, 10605 | |
Contact: Adam J Savitz, MD, PhD 914-997-4394 ads9002@med.cornell.edu | |
Contact: Judith M English, MA 914 682 6974 jme2003@med.cornell.edu | |
Principal Investigator: Adam J Savitz, MD, PhD | |
Sub-Investigator: Judith M English, MA | |
Sub-Investigator: Leeann Grant, BA | |
Weill Medical College of Cornell University | Recruiting |
New York, New York, United States, 10065 | |
Contact: Jason Kim, MD 212-821-0712 jak9001@med.cornell.edu | |
Contact: Judith M English, MA 914 682 6974 jme2003@med.cornell.edu | |
Principal Investigator: Jason Kim, MD | |
Sub-Investigator: Judith M English, MA |
Principal Investigator: | Adam J Savitz, MD, PhD | Weill Medical College of Cornell University |
Responsible Party: | Weill Cornell Medical College ( Adam J Savitz, MD, PhD ) |
Study ID Numbers: | PRE0504007841, 528-444 |
Study First Received: | February 1, 2008 |
Last Updated: | February 13, 2008 |
ClinicalTrials.gov Identifier: | NCT00615511 |
Health Authority: | United States: Institutional Review Board |
schizophrenia schizoaffective disorder negative symptoms cognition |
Schizophrenia Mental Disorders Psychotic Disorders Schizophrenia and Disorders with Psychotic Features |