Can a single dose of an antipsychotic disrupt blood sugar control?
NCT ID NCT00910988
First seen Sep 04, 2026 · Last updated Sep 04, 2026
Summary
This trial tests whether a single dose of the antipsychotic drugs olanzapine or ziprasidone changes how the body responds to insulin, compared with a placebo. The study enrolls healthy young men who are overweight or have early signs of insulin resistance, but who have never taken antipsychotics. Researchers measure insulin sensitivity in the whole body, liver, muscle, and fat tissue to see if olanzapine, but not ziprasidone, causes an acute decrease. The findings could help explain why some antipsychotics raise the risk of diabetes and high blood sugar.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- olanzapine and ziprasidone, two antipsychotic drugs, compared against a placebo
- What this could lead to
- If olanzapine impairs insulin sensitivity more than ziprasidone, it could guide doctors toward antipsychotics with fewer metabolic side effects.
- What could go wrong
- This is a small, early-stage study in healthy men, not patients, so results may not reflect real-world use. The drugs may also cause drowsiness or other side effects.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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46 people
The number who actually took part.
- Start date
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Feb 2009
- Finished
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Jun 2012
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 45 years
- Sex
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Male participants only
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Males aged 18-45 years * BMI approximately ≥ 25 and \< 35 * insulin approximately ≥ 15 µU/ml or triglyceride approximately ≥ 130 mg/dl Exclusion Criteria: * Any DSM-IV Axis I diagnosis * prisoners * any serious medical disorder (i.e. metabolic diseases, type 1 or 2 diabetes mellitus, endocrine disease, coagulopathy, clinically significant anemia, acute infection) * taking prescription medications * non-sedentary lifestyle with \> 3 hours of exercise per week
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Washington University School of Medicine
St Louis, Missouri, 63110, United States
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