Clinical Trials Directory

Trials / Completed

CompletedNCT00910988

Healthy Volunteers Study of the Effects of Olanzapine and Ziprasidone

A Randomized Comparison of the Acute Effects of Olanzapine and Ziprasidone on Whole Body Insulin Sensitivity in Healthy Volunteers

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
46 (actual)
Sponsor
Washington University School of Medicine · Academic / Other
Sex
Male
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

Primary Aim: To test the acute effects of olanzapine or ziprasidone administration, in comparison to placebo, on insulin sensitivity in antipsychotic-naïve healthy young men, measured as whole-body dextrose infusion rates (mg/kg/min), hepatic glucose production (glucose rate of appearance \[Ra\]), primarily muscle glucose utilization (glucose rate of disappearance \[Rd\]), and adipose tissue related free fatty acid production (glycerol rate of appearance \[Ra\]). We hypothesize that olanzapine, but not ziprasidone, will result in acute decreases in insulin sensitivity. Secondary Aim: To test the acute effects of olanzapine or ziprasidone on insulin signaling pathways in antipsychotic naïve healthy young men. We hypothesize that olanzapine, but not ziprasidone, will result in acute alterations in insulin signaling.

Detailed description

See brief description

Conditions

Interventions

TypeNameDescription
DRUGOlanzapineolanzapine/Zyprexa
DRUGZiprasidoneziprasidone/Geodon

Timeline

Start date
2009-02-01
Primary completion
2012-06-01
Completion
2012-06-01
First posted
2009-06-01
Last updated
2018-07-18
Results posted
2014-01-15

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00910988. Inclusion in this directory is not an endorsement.