NCT06605300

Brief Summary

The main aim of the study is to investigate whether intranasal oxytocin and vasopressin have effects on delta-beta cross-frequency coupling under resting-state and task conditions.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
120

participants targeted

Target at P75+ for not_applicable healthy

Timeline
Completed

Started Oct 2024

Geographic Reach
1 country

2 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 18, 2024

Completed
2 days until next milestone

First Posted

Study publicly available on registry

September 20, 2024

Completed
12 days until next milestone

Study Start

First participant enrolled

October 2, 2024

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 28, 2025

Completed
15 days until next milestone

Study Completion

Last participant's last visit for all outcomes

August 12, 2025

Completed
Last Updated

October 3, 2025

Status Verified

September 1, 2025

Enrollment Period

10 months

First QC Date

September 18, 2024

Last Update Submit

September 29, 2025

Conditions

Keywords

oxytocinvasopressindelta-beta coupling

Outcome Measures

Primary Outcomes (3)

  • Resting-state EEG

    Participants are asked to sit comfortably and look at a white cross fixation against a black background on the computer monitor for 15 minutes with delta-beta cross-frequency coupling as a main index.

    35-50 minutes after treatment administration.

  • Behavioral indices in the tasks

    Reaction time and accuracy are recorded in the emotional Stroop and Go/Nogo tasks. For the anxiety induction task, participants are instructed to rate their anxiety levels using a 9-point Likert scale within 4 seconds (1 = not at all, 9 = very anxious).

    50-90 minutes after treatment administration.

  • Task-based EEG

    EEG data are recorded in the emotional Stroop, Go/Nogo, and anxiety induction tasks. Delta-beta cross-frequency coupling will be calculated to do statistical analyses.

    50-90 minutes after treatment administration.

Secondary Outcomes (1)

  • SCR in anxiety induction

    70-90 minutes after treatment administration.

Study Arms (3)

oxytocin

EXPERIMENTAL

A single dose of 24 international units (IU) of oxytocin will be administered with 3 puffs of treatment to each nostril.

Drug: Intranasal Oxytocin (IN-OXT)

vasopressin

EXPERIMENTAL

A single dose of 20 international units (IU) of vasopressin will be administered with 3 puffs of treatment to each nostril.

Drug: Intranasal Vasopressin (AVP)

placebo

PLACEBO COMPARATOR

A single dose of placebo will be administered with 3 puffs of treatment to each nostril.

Drug: Intranasal Placebo

Interventions

Subject assigned to receive intranasal administration of oxytocin (24 IU).

oxytocin

Subjects assigned to receive intranasal administration of vasopressin (20 IU).

vasopressin

Subjects assigned to receive intranasal administration of placebo.

placebo

Eligibility Criteria

Age18 Years - 30 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Healthy subjects without past or current psychiatric or neurological disorders.

You may not qualify if:

  • History of head injury.
  • Pregnant,menstruating,taking oral contraceptives.
  • Medical or psychiatric illness.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

University of Electronic Science and Technology of China

Chengdu, Chengdu, 611731, China

Location

University of Electronic Science and Technology of China (UESTC)

Chengdu, Sichuan, 611731, China

Location

MeSH Terms

Conditions

Diabetes Insipidus

Condition Hierarchy (Ancestors)

Kidney DiseasesUrologic DiseasesFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesMale Urogenital DiseasesPituitary DiseasesEndocrine System Diseases

Study Officials

  • Shuxia Yao, Dr

    University of Electronic Science and Technology of China

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, INVESTIGATOR
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

September 18, 2024

First Posted

September 20, 2024

Study Start

October 2, 2024

Primary Completion

July 28, 2025

Study Completion

August 12, 2025

Last Updated

October 3, 2025

Record last verified: 2025-09

Data Sharing

IPD Sharing
Will not share

Locations