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
| Type | Name | Description |
|---|---|---|
| DRUG | Oxytocin | Single dose intranasal oxytocin (24 IU) |
| DRUG | Placebo | Placebo- 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
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT01614093. Inclusion in this directory is not an endorsement.