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Clinical Trial Summary

The objective of the study is to compare the efficacy of intranasal oxytocin versus intranasal placebo to improve symptoms in schizophrenia patients who have residual symptoms despite being on adequate treatment with antipsychotic medication.


Clinical Trial Description

This is two-site clinical study taking place at UCSD and UCI. Approximately 71 patients at each site will be randomly assigned to either intranasal oxytocin or vehicle placebo at this site.

The total duration for each individual subject will be 6 weeks on study medication (placebo or oxytocin). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01621737
Study type Interventional
Source University of California, San Diego
Contact
Status Terminated
Phase N/A
Start date June 2011
Completion date December 2018

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