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| Sponsor: | University of North Carolina, Chapel Hill |
|---|---|
| Collaborator: |
Eli Lilly and Company |
| Information provided by: | University of North Carolina, Chapel Hill |
| ClinicalTrials.gov Identifier: | NCT00287352 |
Purpose
Weight gain associated with antipsychotic medication use is a major side effect that limits the tolerability of these drugs. This often significant weight gain adversely affects health, increasing risks for developing cardiovascular disease, diabetes, sleep apnea, cancers of the colon, kidneys, uterus, endometrium and esophagus and osteoarthritis. Beasley and colleagues (1997) reported that 40.5% of olanzapine-treated patients gained more than 7% of baseline weight. Much of the olanzapine induced weight gain occurs early in treatment, and antipsychotic-naïve and young patients (Woods et al., 2002) are particularly vulnerable to this side effect. One of the most promising medications to aid weight loss in patients taking olanzapine is amantadine.
Attempts at preventing weight gain are expected to be more successful than attempts to reverse it once it occurs. It is now common clinical practice to educate all patients beginning treatment with olanzapine, and other antipsychotics, about healthy eating and the need for exercise. However, despite this effort, weight gain in this population continues. Beginning a weight-stabilizing medication after a low threshold of weight gain has occurred may have significant impact on patients' health and their willingness to continue to take antipsychotics.
We propose to investigate the efficacy of amantadine as a weight-stabilizing agent in a population of first-episode psychotic subjects just beginning treatment with antipsychotic agents. This population is generally young and medically healthy, without contraindications to amantadine. They are often of normal body mass index and without obesity-related medical problems. They have much to gain in preventing the weight gain which so often progresses steadily over the course of treatment, is difficult to reverse and results in significant morbidity and mortality. Additionally, the first episode psychotic population tends to take fewer concomitant psychiatric medications. This is important since these medications may cause weight gain (long term use of mirtazapine, lithium, depakote) or weight loss (short term use of SSRI's) which could confound the effectiveness of amantadine to combat weight gain.
| Condition | Intervention | Phase |
|---|---|---|
|
Psychotic Disorder Schizophreniform Disorder Schizophrenia Schizoaffective Disorder Mood Disorders With Psychotic Features |
Drug: Olanzapine, Amantadine Drug: Olanzapine and placebo |
Phase I |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Investigator) Primary Purpose: Treatment |
| Official Title: | Double Blind Placebo Controlled Investigation of Amantadine for Retarding Weight Gain in First Episode Adlt Psychotic Subjects Beginning Therapy With Olanzapine. |
| Enrollment: | 40 |
| Study Start Date: | May 2005 |
| Study Completion Date: | September 2009 |
| Primary Completion Date: | September 2009 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Placebo Comparator: Double-Blind Treatment
Olanzapine continuing with placebo
|
Drug: Olanzapine and placebo
Olanzapine continuing as clinically indicated
|
|
Active Comparator: Olanzapine, Amantadine
Standard combine with Amantadine
|
Drug: Olanzapine, Amantadine
Olanzapine continuing as clinically indicated, Amantadine 100 mg tid
|
Show Detailed Description
Eligibility| Ages Eligible for Study: | 18 Years to 65 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Less than 12 weeks of olanzapine monotherapy treatment at entrance into phase 1.
Exclusion Criteria:
Contacts and Locations| United States, North Carolina | |
| University of North Carolina at Chapel Hill | |
| Chapel Hill, North Carolina, United States, 27599 | |
| Principal Investigator: | Karen A Graham, MSc MD | University of North Carolina, Chapel Hill |
More Information
| Responsible Party: | Karen A. Graham, Msc, MD/Principal Investigator, University of North Carolina at Chapel Hill |
| ClinicalTrials.gov Identifier: | NCT00287352 History of Changes |
| Other Study ID Numbers: | F1D-MC-X273, GCRC 2235 |
| Study First Received: | February 3, 2006 |
| Last Updated: | April 29, 2011 |
| Health Authority: | United States: Institutional Review Board |
|
First episode psychosis |
|
Psychotic Disorders Mental Disorders Schizophrenia Mood Disorders Schizophrenia and Disorders with Psychotic Features Amantadine Olanzapine Antiparkinson Agents Anti-Dyskinesia Agents Central Nervous System Agents Therapeutic Uses Pharmacologic Actions Antiviral Agents Anti-Infective Agents Dopamine Agents |
Neurotransmitter Agents Molecular Mechanisms of Pharmacological Action Physiological Effects of Drugs Analgesics, Non-Narcotic Analgesics Sensory System Agents Peripheral Nervous System Agents Antipsychotic Agents Tranquilizing Agents Central Nervous System Depressants Psychotropic Drugs Serotonin Uptake Inhibitors Neurotransmitter Uptake Inhibitors Serotonin Agents Antiemetics |