Actively Recruiting

Phase 2
Age: 21Years - 55Years
All Genders
Healthy Volunteers
NCT06118567

Effect of Nitrous Oxide on Aggression.

Led by Ohio State University · Updated on 2025-03-27

50

Participants Needed

1

Research Sites

260 weeks

Total Duration

On this page

Sponsors

O

Ohio State University

Lead Sponsor

N

National Institute of Mental Health (NIMH)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this experimental medicine clinical trial is to test the hypothesis that nitrous oxide inhalation will result in a change in neurocircuit function in healthy controls and in individuals with impulsive aggressive tendencies. The main question aims to answer are: Does Nitrous Oxide normalize brain circuit function in impulsively aggressive individuals 24 hours after inhalation. Participants will undergo a 60 minute inhalation session with 50% Nitrous Oxide (or room air at another session) and then undergo an fMRI scan 24 hours later. Researchers will compare healthy controls and impulsively aggressive individuals to see if Nitrous Oxide can normalize the function of cortico-limbic circuits in the latter group.

CONDITIONS

Official Title

Effect of Nitrous Oxide on Aggression.

Who Can Participate

Age: 21Years - 55Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Between 21 and 55 years of age
  • Physically healthy with no significant medical conditions
  • Able to give informed consent
  • For IED participants: meet current DSM-5 criteria for IED
  • For IED participants: have LHA aggression scores greater than 12
  • For IED participants: no history of psychosis, bipolar disorder, developmental disorder, intellectual disability, or current substance use disorder
  • For healthy controls: no current or lifetime DSM-5 psychiatric disorder
  • For healthy controls: LHA aggression scores less than 12
Not Eligible

You will not qualify if you...

  • PCL Screening Version Score greater than 13 (likely psychopathic)
  • Current DSM-5 Major Depressive Episode
  • History of bipolar disorder, schizophrenia, or organic mental syndrome
  • Intellectual disability (IQ less than 70)
  • History of nitrous oxide abuse or dependence
  • Clinically significant medical condition
  • Current moderate or severe alcohol or drug use disorder not in full remission
  • Use of antipsychotic medication within the past two weeks
  • Unwilling or unable to sign informed consent

AI-Screening

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Trial Site Locations

Total: 1 location

1

Ohio State University Wexner Medical Center

Columbus, Ohio, United States, 43210

Actively Recruiting

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Research Team

J

Jayla Copland, B.A.

CONTACT

J

Julian Roberts, R.N.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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