Clinical Trials Directory

Trials / Completed

CompletedNCT01614093

Effects of Intranasal Oxytocin on Satiety Signaling in People With Schizophrenia

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
24 (actual)
Sponsor
University of Maryland, Baltimore · Academic / Other
Sex
All
Age
18 Years – 54 Years
Healthy volunteers
Not accepted

Summary

The objective of this study is to test a single dose of intranasal oxytocin, compared to placebo, in a within subjects, crossover design, to see if oxytocin will improve satiety signaling (behaviorally and/or by self report) compared to placebo. If this single dose pilot paradigm shows an increase in satiety, it may be tested in follow-up studies as a prevention or treatment for weight gain and overeating in people with schizophrenia.

Conditions

Interventions

TypeNameDescription
DRUGOxytocinSingle dose intranasal oxytocin (24 IU)
DRUGPlaceboPlacebo- Sugar pill

Timeline

Start date
2012-06-01
Primary completion
2014-01-01
Completion
2014-01-01
First posted
2012-06-07
Last updated
2019-08-28
Results posted
2017-09-21

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT01614093. Inclusion in this directory is not an endorsement.

Effects of Intranasal Oxytocin on Satiety Signaling in People With Schizophrenia (NCT01614093) · Clinical Trials Directory