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Clinical Trial Summary

The main aim of the study is to investigate whether intranasal oxytocin (24IU) influences reward sensitivity and performance monitoring during reinforcement learning.


Clinical Trial Description

A double-blind, within-subject, placebo-controlled pharmacological EEG design will be employed. A total of 35 healthy male subjects will be recruited which will receive either intranasal placebo or oxytocin (24IU) on two separate study days (order counter-balanced, washout period at least 2 weeks). 45 minutes after treatment subjects will undergo a probabilistic feedback reinforcement learning paradigm with concurrent EEG acquisition. During the paradigm subjects will learn the reward probabilities of two different visual stimuli from probabilistic feedback provided by social stimuli (positive, negative emoticon). The paradigm includes an initial acquisition phase and a subsequent test phase. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03846271
Study type Interventional
Source University of Electronic Science and Technology of China
Contact Zhuang Qian, MD
Phone 13086663679
Email zq19910362@126.com
Status Recruiting
Phase N/A
Start date December 4, 2018
Completion date July 31, 2019

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