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WithdrawnNCT01123317Updated Aug 19, 2019

Brain Blood Flow Changes Elicited by Oxytocin in Volunteers With and Without Schizophrenia

An interventional study of Oxytocin in Schizophrenia, sponsored by University of Maryland, Baltimore. Withdrawn at 1 site in United States. Open to participants aged 18 Years to 55 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2019-08-19.

Sponsored by University of Maryland, Baltimore · Not applicable, Interventional, and Basic science

Why this study was withdrawn
Never started
Phase
Not applicable
Study type
Interventional
Enrollment
0
Allocation
Not applicable
Ages
18 Years to 55 Years
Sex
All
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Study summary

The purpose of this study is to assess how oxytocin delivered intranasally changes regional brain blood flow measured by positron emission tomography (PET) in conjunction with oxygen-15 labeled water in persons with schizophrenia. The objective is to better our understanding of oxytocin's role in the modulation of social judgment in schizophrenia and provide more information as to potential uses of oxytocin or a similar drug analog in treating certain features of schizophrenia and other neuropsychiatric disorders.

Read the detailed description

Schizophrenia is a severely debilitating psychiatric disorder that afflicts approximately 1% of the population (American Psychiatric Association, 1994) and is a serious public health problem. The specific mechanism of schizophrenia remains unknown. Affective responsivity and adaptive social behaviors are fundamental impairments in people with schizophrenia. These features have a detrimental impact on function in many areas of daily life. Unfortunately, the brain mechanisms that underlie these problems are still not understood. This study will use positron emission tomography (PET) and regional cerebral blood flow (rCBF) measures to ascertain the timing (1.5 hour period) of OT action on absolute regional brain activity in schizophrenia (SZ) and healthy control (HC) subjects. Particular focus will be on the amygdala, ventral striatum, anterior hippocampus and hypothalamus (neural regions involved in affliative behavior). Subjects will be studied with intranasally administered oxytocin and placebo while at rest and while making judgments about emotional faces. This approach will tell us to what extent the amygdala and limbic system's physiological response to oxytocin is predictive of a subject's behavioral sensitivity to this neuropeptide. The elucidation of this information may have a significant impact on predicting functional outcome and novel drug treatments in schizophrenia.

Functional magnetic resonance imaging (MRI) studies show that oxytocin modulates the amygdala's response during social and emotional decisions. When administered intranasally, OT may be beneficial for the treatment of negative symptoms in schizophrenia by enhancing a person's affiliative behavior and diminishing distrust. It is not, however, known to what extent intranasal oxytocin modifies regional neurotransmission and human brain metabolism. There are at present no studies in animals or humans specifically examining the time course action of OT on whole brain activity.

02

Conditions studied

  • Schizophrenia

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Keywords

  • Schizophrenia
  • PET
  • Oxytocin
03

In context

Schizophrenia

3,472 studies on the registry are indexed under Schizophrenia; 472 are open to participants now.

Browse Schizophrenia studies →

Lead sponsor

University of Maryland, Baltimore is the lead sponsor of 687 studies on the registry; 129 are open to participants now.

Of its 90 completed or terminated interventional studies of FDA-regulated products, 63 (70%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 55 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Normal volunteers: Age range: 18-55 years of age
  • Normal Volunteers: No psychiatric illness in self; no psychotic illness in first degree relatives
  • Normal Volunteers: No previous history of substance dependence in last 6 months; no substance abuse in last month
  • Normal Volunteers: No contraindication for MRI scanning (i.e. cardiac pacemaker, prosthesis)
  • Normal Volunteers: Not pregnant
  • Normal Volunteers: No major medical illness (e.g. seizure disorder) or medication that affects brain structure (e.g. steroids)
  • Normal Volunteers: Participation in Healthy Subject Recruitment protocol (HP-00042350).
  • Patient Volunteers: DSM-IV diagnosis of schizophrenia
  • Patient Volunteers: Voluntary and competent to sign an informed consent
  • Patient Volunteers: No contraindication for MRI scanning (i.e. cardiac pacemaker, prosthesis)
  • Patient Volunteers: No previous history of substance dependence in last 6 months; no substance abuse in last month
  • Patient Volunteers: Not pregnant
  • Patient Volunteers: No major medical illness other than schizophrenia that affects brain structure (e.g. seizure disorder); not currently taking medication other than that for schizophrenia that affects brain structure (e.g. steroids)
  • Patient Volunteers: No diagnosis of Major Depressive Disorder within last 6 months
  • Patient Volunteers: SANS Asociality global score 2 or greater
  • Patient Volunteers: No change in antipsychotic medication (type and dose) within the last 4 weeks
  • Patient volunteers: Age range: 18-55 years of age

Exclusion criteria

Exclusion Criteria:

  • Normal Volunteers: Age outside of specified range -Normal Volunteers: Psychiatric illness in self; psychotic illness in first- degree relative
  • Normal Volunteers: Previous history of substance dependence in last 6 months; substance abuse in last month
  • Normal Volunteers: Contraindication for MRI scanning (i.e. cardiac pacemaker, prosthesis)
  • Normal Volunteers: Pregnant
  • Normal Volunteers: Major medical illness (e.g. seizure disorder) or medication that affects brain structure (e.g. steroids)
  • Patient Volunteers: Age outside of specified range
  • Patient Volunteers: Contraindication for MRI scanning (i.e. cardiac pacemaker, prosthesis)
  • Patient Volunteers: History of substance dependence in last 6 months; substance abuse in last month
  • Patient Volunteers: Pregnancy
  • Patient Volunteers: Major medical illness other than schizophrenia that affects brain structure; currently taking medication other than that for schizophrenia that affects brain structure
  • Patient Volunteers: Diagnosis of Major Depressive Disorder within last 6 months
  • Patient Volunteers: SANS Asociality global score \< 2
  • Patient Volunteers: Change in antipsychotic medication (type and dose) within the last 4 weeks
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Not applicable
Intervention model
Single group
Masking
Single
Enrollment
0 participants (actual)

Study arms

  • Experimental
    Oxytocin

    Subjects will be randomly assigned to either OT-Placebo or Placebo-OT order for PET scan drug administration and will receive the first of the two intranasal doses at Pet scan 1 and the second intranasal dose of the subsequent treatment at Pet Scan 2

    Drug: Oxytocin

Interventions

  • DrugOxytocin

    Subjects will be randomly assigned to either OT-Placebo or Placebo-OT order for PET scan drug administration and will receive the first of the two intranasal doses at Pet scan 1 and the second intranasal dose of the subsequent treatment at Pet Scan 2

    Also known as: Syntocinon

06

What researchers measure

Primary outcomes

  1. Oxytocin induced rCBF changes

    Oxytocin induced rCBF changes in the amygdala, ventral striatum, hypothalamus and anterior hippocampus (post-drug versus pre-drug, resting and task conditions

    Time frame: 2 years

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Study locations

1 site
  • Maryland Psychiatric Research Center
    Catonsville, Maryland 21228, United States
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 19, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01123317
Lead sponsor
University of Maryland, Baltimore
Responsible party
Robert Buchanan (Director, Maryland Psychiatric Research Center, University of Maryland, Baltimore) — Principal investigator
First posted
May 14, 2010
Start date
Jul 2010
Primary completion
Jan 2011 (estimated)
Completion
Jan 2013 (estimated)
Last update
Aug 19, 2019

Study contacts

Henry Holcomb, M.D.
principal investigator · MPRC

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Aug 2019. You cannot join it, but the record below documents what was studied.

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