CClinicalTrials.gg
Status unknownNCT04493515Updated Jul 30, 2020

Oral Oxytocin's Effects on Attention Control

An interventional study of Oral Oxytocin and Oral Placebo in Healthy, sponsored by University of Electronic Science and Technology of China. Status unknown at 1 site in China. Open to male participants aged 18 Years to 30 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2020-07-30.

Sponsored by University of Electronic Science and Technology of China · Not applicable, Interventional, and Basic science

The sponsor has not verified this record recently (last verified Jul 2020), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
80
Allocation
Randomized
Ages
18 Years to 30 Years
Sex
Male
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Study summary

The main aim of the study is to investigate whether orally administered oxytocin (24IU) could modulate attention control using a social-emotional saccade/antisaccade eye-tracking paradigm.

Read the detailed description

Numerous studies have reported the effect of intranasally administered oxytocin on attentional processing including stimulus-driven bottom-up processing and top-down goal-directed inhibitory control. However, it is unclear whether the functional effects are mediated by the peptide directly entering the brain or indirectly via raising peripheral concentrations. One possible method of producing a similar pattern of increased peripheral oxytocin concentrations but without the possibility of direct entry into the brain would be to administer the peptide lingually. In the present double-blind, between-subject, placebo-controlled study, 80 healthy male subjects will be recruited and receive either oxytocin (24IU) or placebo control administered orally (lingual). 45 minutes after treatment subjects are required to complete a social-emotional saccade/antisaccade eye-tracking paradigm. This paradigm uses social (happy, sad, angry, fear, and neutral faces) as well as non-social (oval shapes) stimuli to explore social- and emotion-specific effects of orally administered oxytocin.

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Conditions studied

  • Healthy
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In context

Lead sponsor

University of Electronic Science and Technology of China is the lead sponsor of 109 studies on the registry; 35 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 30 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes

Inclusion criteria

  • Male, healthy participants
  • Non smokers

Exclusion criteria

Exclusion Criteria:

  • Previous or current medical, psychiatric, neurological disorder
  • Regular medication
  • Use of any psychoactive substances in the 24 hours before experiment
  • Contra-indications for oxytocin
  • Contra-indications for eye-tracking data acquisition
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Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Investigator, Outcomes assessor)
Enrollment
80 participants (estimated)

Study arms

  • Experimental
    Oral Oxytocin

    Oxytocin orally (24 IU)

    Drug: Oral Oxytocin

  • Placebo comparator
    Oral Placebo

    Placebo orally (24 IU, identical ingredients, except the active agent)

    Drug: Oral Placebo

Interventions

  • DrugOral Oxytocin

    Administration of oxytocin orally (24 IU)

  • DrugOral Placebo

    Administration of placebo orally (24 IU)

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What researchers measure

Primary outcomes

  1. Effect of oral oxytocin administration on saccade/antisaccade latencies towards social (facial) versus non-social (shape) stimuli

    Comparison between social-specific saccade/antisaccade latencies (in milliseconds) between the oxytocin and placebo treatment conditions

    Time frame: 45 minutes - 100 minutes after treatment

  2. Effect of oral oxytocin administration on error rates of saccade/antisaccade for social (facial) versus non-social (shape) stimuli

    Comparison between social-specific error rates of saccade/antisaccade between the oxytocin and placebo treatment conditions.

    Time frame: 45 minutes - 100 minutes after treatment

Secondary outcomes

  1. Emotion-specific effects of oral oxytocin administration on saccade/antisaccade latencies towards the separate facial emotions

    Comparison between emotion-specific saccade/antisaccade latencies (in milliseconds) between the oxytocin and placebo treatment conditions

    Time frame: 45 minutes - 100 minutes after treatment

  2. Emotion-specific effects of oral oxytocin administration on saccade/antisaccade error rates for the separate facial emotions

    Comparison between emotion-specific saccade/antisaccade error rates between the oxytocin and placebo treatment conditions

    Time frame: 45 minutes - 100 minutes after treatment

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Study locations

1 of 1 sites recruiting
  • University of Electronic Science and Technology of China(UESTC)
    Chengdu, Sichuan 611731, China
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 30, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04493515
Lead sponsor
University of Electronic Science and Technology of China
Responsible party
Keith Kendrick (Professor, University of Electronic Science and Technology of China) — Principal investigator
First posted
Jul 30, 2020
Start date
Jul 28, 2020
Primary completion
Dec 31, 2020 (estimated)
Completion
Dec 31, 2021 (estimated)
Last update
Jul 30, 2020

Study contacts

Zhuang Qian, MD
Contact
zq19910362@126.com
13086663679
Xu Xiaolei, PhD
Contact
rabby_uestc@outlook.com
18780140034
Keith Kendrick, PhD
principal investigator · University of Electronic Science and Technology of China (UESTC)

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jul 2020. You cannot join it, but the record below documents what was studied.

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