Strategies to Reduce Antipsychotic-Associated Weight Gain in Youth
Completed · Phase 2 · Has a placebo group
Conditions studied: Weight Gain
In brief
The purpose of this pilot study is to determine whether starting metformin in conjunction with a second-generation antipsychotic (SGA) and providing information about healthy eating and activity will prevent or reduce the amount of weight gain and the metabolic changes in adolescent youth typically seen with second-generation antipsychotic medication.
Key facts
- Study ID
- NCT00617240
- Run by
- University of North Carolina, Chapel Hill
- People needed
- 9
- Starts
- 2007-01-01
- Expected to finish
- 2012-10-01
- Last updated by the study team
- 2014-03-11
Who can join
Age: 10 and older, up to 17. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Subjects will be between the ages of 10 and 17, male or female, any race or ethnicity
- Any SPMI pediatric diagnosis that meets DSM-IV criteria and frequently is treated with a SGA- typically but not limited to psychotic, mood, pervasive developmental, oppositional defiant, and conduct disorders
- SGA-naïve or less than 2 weeks exposure to any SGA, except ziprasidone
- Legal guardian able and willing to give written informed consent
- If competent, subject able and willing to assent for their own participation
You may not qualify if…
- Previous trial of metformin
- Recommendation for treatment with clozapine or ziprasidone
- Current use of insulin or any oral hypoglycemic agent
- Current use of a medication known to mitigate weight gain - amantidine, histamine (H2) antagonists (cimetidine, ranitidine, nizatidine), topiramate, orlistat, sibutramine, stimulants (dextroamphetamine, methylphenidate)
- Any current or past diagnosis of an eating disorder
- Diabetes mellitus
- Current active thyroid (TSH >18 microIU/ml; T4 total >18 mcg/dl), hepatic (2 LFTs >4x upper limits of normal), renal (serum Creatinine >1.4 mg/dL in females and serum Creatinine >1.5 mg/dL in males), cardiac, gastrointestinal, or adrenal disease
- Current substance abuse/dependence within past 2 weeks; a positive urine tox screen at baseline in the absence of meeting criteria for abuse/dependence will not preclude enrollment.
- Pregnancy or breast feeding
Where it is running
- University of North Carolina, Department of Psychiatry — Chapel Hill, North Carolina, United States
Full record on ClinicalTrials.gov
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