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Clinical Trials in China / NCT07140237
Recruiting Phase EARLY_PHASE1

The Effect of Oral Oxytocin and Atosiban on Top-down Attention ( OTAtosiban )

NCT07140237 · tracked via the Priya Life Science China tracker
Sponsor
University of Electronic Science and Technology of China
Phase
Phase EARLY_PHASE1
Started
2025-09
Last updated
2025-09-08

Condition(s) studied

Healthy Adult Male

Investigational drug(s) / intervention(s)

Oxytocin lower does (24IU)Oxytocin higher does (48IU)AtosibanPlacebo

Oxytocin lower does (24IU): Oxytocin (24IU) will be administered as a lingual spray (6, 0.1puffs (4IU per puff) of spray on and under the tongue)

Oxytocin higher does (48IU): Oxytocin (48IU) will be administered as a lingual spray (6, 0.1ml sprays (8IU per puff) on and under the tongue)

Atosiban: 150ug atosiban administered by lingual sprays (6, 0.1ml sprays on and under the tongue)

Placebo: Placebo administered as a lingual spray (6, 0.1puffs (4IU per puff) of spray on and under the tongue). Placebo has the same composition of 0.9% saline and glycerol as for oxytocin and the atosiban interventions.

Study summary

The main aim of the present study is to investigate whether orally (lingual spray) administered oxytocin influences human top-down attention via oxytocin receptors and whether its effects are dose- and task-dependent.

Eligibility

Sex
MALE
Min age
18 Years
Max age
35 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Healthy male subjects without past or current psychiatric or neurological disorders Exclusion Criteria: * History of or current neurological/psychiatric disorders; * Use of psychotropic medications (including nicotine) * Visual impairments

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
School of Life science and Technology, University of Electronic Science and Technology of China Chengdu Sichuan Recruiting

More University of Electronic Science and Technology of China trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07140237 on ClinicalTrials.gov ↗ ← All trials in China