Metabolic Effects of Antipsychotics in Children
- Registration Number
- NCT00205699
- Lead Sponsor
- Washington University School of Medicine
- Brief Summary
The project aims to describe and compare the outcome of 12 weeks of prospective, randomized treatment with olanzapine, risperidone or aripiprazole on insulin action in skeletal muscle, liver and adipose tissue, abdominal fat mass, total body and fat-free mass, efficacy for symptoms of aggression and non-metabolic adverse events. Children aged 6-18 will be st...
- Detailed Description
This randomized clinical trial assesses both the safety and efficacy of atypical antipsychotic agents in antipsychotic-naive aggressive children with various childhood psychiatric disorders during 12 weeks of prospective, randomized treatment with olanzapine, risperidone or aripiprazole.
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Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 144
- Aged 6-18 years
- Generally healthy and a score of ≥ 18 on the Aberrant Behavior Checklist in the context of one or more Axis I Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV) childhood psychiatric disorders, including conduct disorder, oppositional defiant disorder, disruptive behavior disorder, autism, pervasive developmental disorder, attention deficit disorder, schizophrenia and bipolar affective disorders
- Children's Global Assessment Scale (CGAS) score ≤ 60
- Not previously treated with an antipsychotic; individual subjects with remote, brief prior antipsychotic exposure may be considered for enrollment by the PI on a case by case basis
- Patient assent and informed consent obtained from the parent or guardian
- No clinically significant (based on PI determination) changes in permitted medications (e.g., stimulants and selective serotonin reuptake inhibitors [SSRIs]) for approximately 1 month prior to Baseline evaluations
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Active suicidality or primary dx of major depressive disorder
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Any lifetime use of antipsychotics or non-serotonin selective reuptake inhibitor (non-SSRI) anti-depressants
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The presence of any serious medical disorder, based on PI determination, that may confound the assessment of relevant biologic measures or diagnoses, including:
- significant organ system dysfunction;
- endocrine disease, including type 1 or type 2 diabetes mellitus;
- coagulopathy;
- anemia;
- or acute infection.
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Subjects regularly taking any glucose lowering agent, lipid lowering agent, exogenous testosterone, recombinant human growth hormone, or any other endocrine agent that might confound substrate metabolism, oral glucocorticoids (glucocorticoid inhalants and nasal sprays are permitted), antihistamines, sedating antihistamines (non-sedating antihistamines such as but not limited to Claritin (loratadine) and Zyrtec (cetirizine) are permitted), and certain mood stabilizing agents, as some medications may themselves worsen or otherwise alter weight gain, glucose and lipid regulation or otherwise make it difficult to assess the effects of the antipsychotic alone; (note that exposure to many psychotropic agents including stimulants and SSRI's is permitted in order to maintain the generalizability of the sample);
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Intelligence quotient (IQ) < 70 (based on school records and/or evaluation by clinician)
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current substance abuse
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Past history or currently has dyskinesia
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Stimulant dosage significantly higher (per PI judgment)than the equivalent of approximately 2mg/kg/day methylphenidate equivalent dose.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description aripiprazole aripiprazole Participants in this group will be randomized to flexibly-dosed treatment with aripiprazole. olanzapine olanzapine Participants in this group will be randomized to flexibly-dosed treatment with olanzapine. risperidone risperidone Participants in this group will be randomized to flexibly-dosed treatment with risperidone.
- Primary Outcome Measures
Name Time Method Change in Insulin-stimulated Glucose Rate of Disappearance (Glucose Rd) 12 weeks This study hypothesized that antipsychotic treatment would decrease insulin sensitivity at muscle, as measured by the insulin-stimulated rate of disappearance of glucose (glucose Rd), with larger adverse effects for olanzapine.
Change in DEXA % Body Fat 12 weeks This study hypothesized that antipsychotic treatment would increase percent total body fat, as measured by whole body dual energy x-ray absorptiometry (DEXA), with larger adverse effects for olanzapine.
- Secondary Outcome Measures
Name Time Method Change in MRI-measured Visceral Abdominal Fat 12 weeks This study hypothesized that antipsychotic treatment would increase visceral abdominal fat, as measured by abdominal magnetic resonance imaging (MRI), with larger adverse effects for olanzapine.
Change in MRI-measured Subcutaneous Abdominal Fat 12 weeks This study hypothesized that antipsychotic treatment would increase subcutaneous abdominal fat, as measured by abdominal magnetic resonance imaging (MRI), with larger adverse effects for olanzapine.
Change in Insulin-stimulated Glycerol Rate of Appearance (Glycerol Ra) 12 weeks This study hypothesized that antipsychotic treatment would decrease insulin sensitivity at adipose tissue, as measured by the insulin-stimulated rate of disappearance of glycerol (glycerol Ra), with larger adverse effects for olanzapine.
Change in Insulin-stimulated Glucose Rate of Appearance (Glucose Ra) 12 weeks This study hypothesized that antipsychotic treatment would decrease hepatic insulin sensitivity, as measured by the rate of appearance of glucose (glucose Ra), with larger adverse effects for olanzapine.
Trial Locations
- Locations (1)
Washington University School of Medicine, Psychiatry Dept.
🇺🇸Saint Louis, Missouri, United States