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Clinical Trial Summary

schizophrenia patients and healthy volunteers will be included. Subjects who meet the inclusion and exclusion criteria for the study will be recruited. After completion of clinical assessments and neuropsychological assessments, all subjects will undergo two fMRI scans. In one scan subjects will receive a single dose of intranasal oxytocin and in another scan, they will receive intranasal saline. The order of administration of oxytocin or saline will be counterbalanced so that they are not administered in the same order to all subjects. Subjects will be blind to the drug administered.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04176835
Study type Interventional
Source National Institute of Mental Health and Neuro Sciences, India
Contact
Status Completed
Phase N/A
Start date April 2016
Completion date September 2019

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