Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07109245

Do Antipsychotics Block Insulin Action in the Brain: is it a Class Effect?

Status
Recruiting
Phase
Phase 4
Study type
Interventional
Enrollment
35 (estimated)
Sponsor
Centre for Addiction and Mental Health · Academic / Other
Sex
All
Age
18 Years – 35 Years
Healthy volunteers
Accepted

Summary

This study aimed at helping researchers understand how a medication called haloperidol can affect insulin action in the brain. Insulin is a hormone in the body that controls sugar levels in part by lowering the amount of glucose produced by the liver. After eating a meal, insulin levels go up in both the blood and the brain. Insulin in the brain has also been shown to affect the way the brain works and processes information (also known as "cognition"). Haloperidol, is an antipsychotic medication used to treat a variety of disorders such as schizophrenia spectrum disorders, bipolar disorder, and major depressive disorder, but long-term use can have metabolic side effects, like weight gain, type 2 diabetes, and cardiovascular disease. The purpose of this study is to investigate how antipsychotic medications, such as haloperidol, which carries the risk of metabolic changes, might interrupt the effect of insulin action in the brain. This will help researchers learn how to potentially reduce metabolic risk for people who take these kinds of medications in the future.

Conditions

Interventions

TypeNameDescription
DRUGHaloperidolThe oral investigational agent haloperidol (Generic Brand: TEVA-HALOPERIDOL) will be self-administered, at night, over 7 days. Haloperidol will be titrated up to 2 mg.
DRUGPlaceboOral placebo, encapsulated and to be taken at an equivalent titration schedule to Haloperidol.
DRUGInsulin LisproA total of 160 IU of intransal insulin (=1.6 mL) will be administered on MRI scanning visits (80 IU = 0.8 mL delivered per nostril). Humalog; Eli Lilly Canada
OTHERSalineA total of 1.6 mL of intranasal saline will be administered on each MRI scanning visit (0.8 mL delivered per nostril).

Timeline

Start date
2025-12-11
Primary completion
2028-08-01
Completion
2028-12-01
First posted
2025-08-07
Last updated
2026-04-02

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT07109245. Inclusion in this directory is not an endorsement.