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Effects of Intranasal Oxytocin and Vasopressin on Social Behavior

Effects of Intranasal Oxytocin and Vasopressin on Social Behavior in Healthy Controls

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01296269
Enrollment
150
Registered
2011-02-15
Start date
2011-04-30
Completion date
Unknown
Last updated
2011-04-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy

Keywords

social cognition, oxytocin, vasopressin, decision making, social decision making

Brief summary

The purpose of this study is to investigate the role of a one-time intranasal administration of the oxytocin, vasopressin, or placebo on prosocial decision making such as cooperation and altruism in a healthy population of student controls.

Interventions

DRUGOxytocin

one-time intranasal administration, 24 International Units, 5 puffs for each nostril

one-time intranasal administration, 20 International Units, 5 puffs in each nostril

DRUGplacebo

contains all the ingredients as in the oxytocin and vasopressin conditions, save for the active ingredient, one time intranasal administration, 5 puffs in each nostril

Sponsors

Hebrew University of Jerusalem
CollaboratorOTHER
Hadassah Medical Organization
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* healthy controls

Exclusion criteria

* Past or present psychiatric, neurological, endocrinological or severe chronic medical illness. * Use of medications or drugs that would interfere with study results. This includes steroids, medications for psychiatric symptoms like anxiety or depression, stimulants, and medications for high blood pressure. Participants will be asked to tell the investigators of any medications or drugs that they are taking. The investigators will consider the drug interactions with oxytocin and vasopressin prior to study, and participants will not be able to participate in the study if the drug interactions could be dangerous. * history of drug or alcohol addiction * Pregnancy or Nursing Status: Because of the risk to an unborn fetus or infant, women who are pregnant or nursing are excluded from this protocol. All females will have a pregnancy test performed no more than 24 hours before each drug administration and will not be able to participate if the pregnancy test is positive.

Design outcomes

Primary

MeasureTime frameDescription
allocations of monetary unitsapproximately 45 minutes after intranasal administration of vasopressin, oxytocin, or placeboParticipants will make decisions regarding the allocation of monetary units between themselves and other participants. We will measure the quantity of monetary units kept for themselves vs. given to other participants

Secondary

MeasureTime frame
mood as measured via the visual analog scaleapproximately one hour and fifteen minutes after administration of oxytocin, vasopressin or placebo

Countries

Israel

Contacts

Primary ContactDavid Mankuta, MD
mankutad@gmail.com972-2-6776484
Backup ContactSalomon Israel, MA
salomon.israel@mail.huji.ac.il972-524789754

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026