Changes in Adiposity, Metabolic Measures From Atypicals to Aripiprazole
Completed · Phase 4
Conditions studied: Schizophrenia, Type 2 Diabetes Mellitus
In brief
This proposal aims to use well-validated methodologies such as dual energy x-ray absorptiometry (DEXA), frequently sampled oral glucose tolerance tests (fsOGTTs), and hyperinsulinemic euglycemic clamps to characterize the metabolic effects of 12 weeks of aripiprazole treatment following chronic pretreatment with olanzapine, quetiapine, risperidone or ziprasidone. We hypothesize that switching to aripiprazole treatment will induce improvements in total body adiposity, inflammation (e.g., high sensitivity C-reactive protein \[hsCRP\]), glucose metabolism (e.g., insulin sensitivity) and lipid metabolism (e.g., fasting plasma triglyceride), in comparison to chronic pretreatment with olanzapine, risperidone and quetiapine.
Key facts
- Study ID
- NCT00205660
- Run by
- Washington University School of Medicine
- People needed
- 51
- Starts
- 2005-02-01
- Expected to finish
- 2009-08-01
- Last updated by the study team
- 2019-01-15
Who can join
Age: 18 and older, up to 60. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Patient meets DSM-IV criteria for Schizophrenia
- 18-60 years of age or older
- Able to give informed consent
- Treated with olanzapine, quetiapine, risperidone or ziprasidone for greater than or equal to 3 months prior to enrollment
You may not qualify if…
- pregnant or breastfeeding women will be excluded
- Meets DSM-IV criteria for substance abuse or dependence within past 6 months
- involuntary legal status (as per Missouri law)
- any serious medical disorder that may confound assessment of symptoms
- subjects taking prescription medications except psychotropic meds
- meets DSM-IV criteria for Mental Retardation (mild or worse)
- Subjects taking tricyclic antidepressants or mood stabilizers
Where it is running
- Washington University School of Medicine — St Louis, Missouri, United States
Full record on ClinicalTrials.gov
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