Oxytocin Levels in Typically Developing Boys

NCT ID: NCT02006381

Last Updated: 2015-09-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

60 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-12-31

Study Completion Date

2015-04-30

Brief Summary

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Measuring basal levels of plasma oxytocin in individuals with typical development across childhood and adolescence using both extracted and unextracted EIA methods.

Detailed Description

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Measuring basal levels of plasma oxytocin in individuals with typical development across childhood and adolescence using both extracted and unextracted EIA methods. This study is necessary since there is great variability in reported plasma oxytocin in typically developing children from other studies as well as up to 1000 fold variability in such levels using different assay procedures. Further existing studies have not clearly described variation in levels with age. all samples will be taken in the afternoon.

Conditions

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Healthy Boys

Study Design

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Observational Model Type

COHORT

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Age 3-6

This will include 10 typically developing boys age 3-6

No interventions assigned to this group

Age 7-12

This will include 10 typically developing boys age 7-12

No interventions assigned to this group

Age 13-17

This will include 10 typically developing boys age 13-17

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Between 3 and 17 years old, inclusive
* Consent of parent or guardian.

Exclusion Criteria

* Female gender
* Evidence of a mental health diagnosis
* Evidence of significant medical condition (ie: renal, cardiovascular or genetic disease)
* First degree family member with an ASD diagnosis
Minimum Eligible Age

3 Years

Maximum Eligible Age

17 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

Yes

Sponsors

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University of North Carolina, Chapel Hill

OTHER

Sponsor Role lead

Responsible Party

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Linmarie Sikich, MD

Associate Professor of Psychiatry

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Linmarie Sikich, MD

Role: PRINCIPAL_INVESTIGATOR

UNC-Chapel Hill

Locations

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University of North Carolina Chapel Hill

Chapel Hill, North Carolina, United States

Site Status

Countries

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United States

Other Identifiers

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13-3288

Identifier Type: -

Identifier Source: org_study_id

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