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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04413786
Other study ID # UESTC-neuSCAN-71
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 14, 2019
Est. completion date December 26, 2021

Study information

Verified date February 2022
Source University of Electronic Science and Technology of China
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To investigate whether intranasal oxytocin (24IU) treatment has a regulatory effect on attentional processing of emotional faces.


Description:

In a placebo-controlled double-blind between-subject design experiment, investigators plan to investigate the effect of oxytocin treatment on attentional processing of emotional faces. Subjects complete questionnaires in Chinese versions before treatment administration, including the Beck Depression Inventory, Autism Spectrum Quotient , Trait Anxiety Inventory, Toronto Alexithymia Scale, Multidimentional Assessment of Interoceptive Awareness. This experiment consists of two tasks including Emotional Face Cue-target Task and Visual Search Task. In the first task, subjects need to make a response to judge the position of target after a cue-target is presented. In the second task, subjects are asked to search the target "U" or inverted "U" placed on the nose of emotional/neutral faces and make an choices based on their oorientation. During these phases, subjects' response accuracy, response time and electrophysiological activity (ERP) are recorded.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date December 26, 2021
Est. primary completion date December 16, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria: - Healthy subjects without past or current psychiatric or neurological disorders. Exclusion Criteria: - history of head injury - medical or psychiatric illness

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
oxytocin treatment
intranasal administration of oxytocin (24IU)
placebo treatment
intranasal administration of placebo (24IU)

Locations

Country Name City State
China School of life science and technology, University of Electronic Science and Technology of China Chengdu Sichuan

Sponsors (1)

Lead Sponsor Collaborator
University of Electronic Science and Technology of China

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Response time in reponse to different emotional face targets. Response time in discriminating which side (left or right) the emotional face target appear. 1 hour
Primary N2pc N2pc is an enhanced negative event-related potential typically elicited at posterior electrodes (e.g., PO7 and PO8) contralateral to the target presented among distractors between 180 and 300 ms after the onset of stimuli.
display.
1 hour
Secondary Response accuracy in response to different emotional face targets. Response accuracy is caculated by the precentage of correct responses among the total responses in discriminating the position (left or right side) of different face conditions. 1 hour
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