Actively Recruiting

Early Phase 1
Age: 18Years - 59Years
All Genders
Healthy Volunteers
NCT06702631

Nitrous Oxide Neuroimaging

Led by Keith M Vogt · Updated on 2026-04-15

60

Participants Needed

1

Research Sites

72 weeks

Total Duration

On this page

Sponsors

K

Keith M Vogt

Lead Sponsor

N

National Institute of General Medical Sciences (NIGMS)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The purpose of this study is to determine the effects of acute pain on long-term memory and conditioned physiologic responses in the presence and absence of low dose nitrous oxide. Functional magnetic resonance imaging will be used to identify the neural correlates of these phenomena. The study will occur over 2 visits and involves no long-term follow up.

CONDITIONS

Official Title

Nitrous Oxide Neuroimaging

Who Can Participate

Age: 18Years - 59Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Have none of the specific exclusion criteria
  • Have a valid email address and phone number throughout the study
  • Free from any non-MRI compatible implants
Not Eligible

You will not qualify if you...

  • Are pregnant or trying to conceive
  • Body mass index (BMI) greater than 35
  • Significant memory impairment or hearing loss
  • Sleep apnea
  • Chronic pain or frequent use of pain medication, including tramadol
  • Any severe or poorly-controlled medical problem such as hypertension or diabetes
  • Neurologic or psychiatric diseases, including anxiety and depression
  • Severe cardiac disease
  • History of methylenetetrahydrofolate reductase (MTHFR) deficiency or variant mutation
  • Recent ear or eye surgery
  • Claustrophobia
  • Have metal implants or non-removable metal piercings
  • History of adverse reactions to anesthetics
  • Daily alcohol or heavy alcohol use; history of alcohol abuse
  • Current daily smoker
  • Regular or recent marijuana use, including prescribed medical marijuana
  • Illicit drug use (street drugs)
  • Regular use of antiepileptics, antidepressants, antipsychotics, antihistamines, anti-anxiety medications, stimulants, or sleep aids

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Pittsburgh

Pittsburgh, Pennsylvania, United States, 15213

Actively Recruiting

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Research Team

K

Keith M Vogt, MD, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

BASIC_SCIENCE

Number of Arms

1

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