CClinicalTrials.gg
CompletedNCT04493554Updated Jan 7, 2021

The Effects of Vasopressin on Attention Control

An interventional study of Vasopressin and Placebo in Healthy, sponsored by University of Electronic Science and Technology of China. Completed at 1 site in China. Open to male participants aged 18 Years to 30 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2021-01-07.

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

Phase
Not applicable
Study type
Interventional
Enrollment
89
Allocation
Randomized
Ages
18 Years to 30 Years
Sex
Male
01

Study summary

The main aim of the present study is to investigate whether intranasal vasopressin (20IU) could influence attention control in a social-emotional saccade/antisaccade eye-tracking paradigm.

Read the detailed description

A number of previous studies have reported vasopressin's effect on human social behavior and social cognition, although it remains unclear whether vasopressin could modulate attention allocation including stimulus-driven bottom-up control and goal-directed top-down control. In the current randomized, between-subject, placebo controlled study, 89 healthy male subjects will be recruited and receive either vasopressin (20 IU) or placebo control administered intranasally. 45 minutes after treatment subjects will be required to complete a social-emotional saccade /antisaccade eye-tracking paradigm. The 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 vasopressin.

02

Conditions studied

  • Healthy
03

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.

04

Who can participate

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

Inclusion criteria

  • 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 vasopressin
  • Contra-indications for eye-tracking data acquisition
05

Study design

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

Study arms

  • Experimental
    Vasopressin

    Vasopressin (20 IU) intranasally

    Drug: Vasopressin

  • Placebo comparator
    Placebo

    Placebo intranasally

    Drug: Placebo

Interventions

  • DrugVasopressin

    Administration of vasopressin (20 IU) intranasally

  • DrugPlacebo

    Administration of placebo intranasally

06

What researchers measure

Primary outcomes

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

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

    Time frame: 45 minutes - 100 minutes after treatment

  2. Effect of vasopressin 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 vasopressin and placebo treatment conditions

    Time frame: 45 minutes - 100 minutes after treatment

Secondary outcomes

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

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

    Time frame: 45 minutes - 100 minutes after treatment

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

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

    Time frame: 45 minutes - 100 minutes after treatment

07

Study locations

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

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 7, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04493554
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
Nov 30, 2020
Completion
Jan 1, 2021
Last update
Jan 7, 2021

Study contacts

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 completed, as verified in Jan 2021. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion