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Sponsors and Collaborators: |
Yale University Stanley Medical Research Institute |
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Information provided by: | Yale University |
ClinicalTrials.gov Identifier: | NCT00268749 |
This is an open label trial of the NMDA agonist glycine used alone for symptoms that appear to be prodromal for schizophrenia in adolescents and young adults.
Condition | Intervention | Phase |
---|---|---|
Schizophrenia |
Drug: glycine Drug: placebo |
Phase II |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Parallel Assignment, Safety/Efficacy Study |
Official Title: | Glycine Treatment of Prodromal Symptoms |
Enrollment: | 6 |
Study Start Date: | July 2002 |
Arms | Assigned Interventions |
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1: Experimental |
Drug: glycine
0.8 g/kg/day
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2: Placebo Comparator |
Drug: placebo
placebo
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Ages Eligible for Study: | 14 Years to 35 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Study ID Numbers: | 02T-175 |
Study First Received: | December 20, 2005 |
Last Updated: | March 25, 2008 |
ClinicalTrials.gov Identifier: | NCT00268749 History of Changes |
Health Authority: | United States: Food and Drug Administration |
Schizophrenia Neurotransmitter Agents Glycine |
Mental Disorders Psychotic Disorders Schizophrenia and Disorders with Psychotic Features |
Schizophrenia Neurotransmitter Agents Molecular Mechanisms of Pharmacological Action Glycine Mental Disorders |
Physiological Effects of Drugs Glycine Agents Pharmacologic Actions Schizophrenia and Disorders with Psychotic Features |