Clinical Trials Directory

Trials / Completed

CompletedNCT01739127

Comparison of Aripiprazole Versus Higher Metabolic Risk Antipsychotic Drugs on Adiposity Using MRI

A Longitudinal Comparison of Aripiprazole vs. Higher Metabolic Risk Antipsychotic Drugs on Adiposity Using MRI

Status
Completed
Phase
Study type
Observational
Enrollment
83 (actual)
Sponsor
University of British Columbia · Academic / Other
Sex
All
Age
12 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to compare abdominal weight gain and fat distribution in people taking aripiprazole versus risperidone or quetiapine, to people not taking any of these antipsychotic medications.

Detailed description

Second generation antipsychotic drugs have much greater efficacy for refractory schizophrenia and have much lower propensity to induce motor side-effects. These medications are seeing increased use for indications other than psychosis, and greater use in populations such as adolescents. However, one of the most critical issues in the field of psychiatry today is the overwhelming evidence that chronic use of the second generation antipsychotics can result in metabolic dysregulation, which includes weight gain, hyperlipidemia, and insulin resistance. A recent meta-analysis indicated that switching from other second generation antipsychotics to the antipsychotic drug aripiprazole consistently resulted in significant weight loss and may be an optimal treatment for patients who exhibit drug-induced weight gain. Therefore, we aim to compare metabolic dysregulation (namely abdominal weight gain and fat distribution)in participants taking aripiprazole, to participants who are taking higher-metabolic propensity antipsychotic drugs (such as risperidone or quetiapine), and to healthy participants.

Conditions

Interventions

TypeNameDescription
DRUGAripiprazoleTo be prescribed and monitored by participant's attending physician (not given to participants as a part of the study).
DRUGRisperidone/QuetiapineTo be prescribed and monitored by participant's attending physician (not given to participants as a part of the study).

Timeline

Start date
2012-11-01
Primary completion
2016-02-01
Completion
2016-02-01
First posted
2012-12-03
Last updated
2016-05-25

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT01739127. Inclusion in this directory is not an endorsement.