NMDA Receptor Antagonist Nitrous Oxide Targets Affective Brain Circuits

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The Washington University

Status and phase

Terminated
Phase 1

Conditions

Depressive Disorder, Treatment-Resistant
Depressive Disorder, Major

Treatments

Device: MRI
Drug: Nitrous Oxide
Drug: Placebo gas

Study type

Interventional

Funder types

Other

Identifiers

NCT02994433
201606120

Details and patient eligibility

About

Most clinical major depression responds to standard treatments (medication and psychotherapy); however, a significant subset of depressed patients (15-20%) do not respond to these treatments and are referred to as treatment-resistant major depression (TRMD). New treatments for TRMD are needed, and one promising line of research are drugs known as N-methyl-D-aspartate (NMDA) glutamate receptor antagonists. In a recent pilot study, our group demonstrated that the NMDA antagonist nitrous oxide is effective in TRMD. This application proposes to take the next important step in understanding how nitrous oxide exerts its effects in the human brain by using state-of-the-art brain neuroimaging (functional connectivity magnetic resonance imaging) in a group of non-depressed, healthy volunteers and comparing the results to a group of TRMD patients. This study involves exposing 20 non-depressed healthy participants and 20 TRMD participants to nitrous oxide and a placebo gas, to compare their brain images before and after each of the inhalation sessions. Sessions will be separated by at least one month to prevent treatment effects from carrying over into the following session. All willing and eligible subjects will undergo up to six functional connectivity MRI scans, and two inhalation sessions. Functional imaging in the brain will allow us to trace the interconnections between various parts of the brain, including those involved with emotion and depression. Other procedures will involve screening materials to ensure safety of the participants before beginning the study (i.e. no MRI scan contraindications) and that subjects meet eligibility criteria to being in the targeted age range, depression/non-depressed state, neurological disorder history, and no medication exclusions.

Enrollment

49 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Adults 18-65 years of age
  • Right-handed
  • Controls: Not meet The Fourth Edition of the Diagnostic and Statistical Manual of Mental Disorders (DSM-IV) criteria for major depressive disorder (MDD) by scoring ≤7 on the Hamilton Depression Rating Scale (HDRS), 17-item; Treatment-Resistant Major Depression (TRMD) patients: Must meet a ≥17 score on the HDRS.
  • Controls: Must not have any history of depression as determined by reported history and medical record review; TRMD: Documented (chart review) failure to respond to ≥3-4 adequate dose/duration antidepressant treatments; ≥1 in the current depressive episode.
  • Good command of the English language

Exclusion criteria

  • Meets criteria for any DSM-IV Axis I diagnosis as documented in medical records and as determined by structured clinical interview (except MDD for the TRMD group)

  • Known primary neurological disorders or medical disorders including dementia, stroke, encephalopathy Parkinson's Disease, brain tumors, multiple sclerosis, seizure disorder, severe cardiac or pulmonary disease

  • Any central nervous system active medication as determined by study investigator

  • Any known disease affecting drug metabolism and excretion (e.g. renal or liver disease) as determined by study investigator

  • Left-handedness

  • Not eligible for MRI scans (e.g. history of claustrophobia/implanted metal as per MRI Screening Tool)

  • Current use of psychotropic medications, antidepressants, or prescription or non-prescription drugs/herbals intended to treat depression or anxiety (control group only)

  • Any recent (within past 12 months) history of substance dependence or abuse, determined by reported history or urine drug screen

  • Ability to become pregnant and not using effective contraception

  • Contraindication against the use of nitrous oxide:

    1. Pneumothorax
    2. Bowel obstruction
    3. Middle ear occlusion
    4. Elevated intracranial pressure
    5. Chronic cobalamin and/or folate deficiency treated with folic acid or vitamin B12
    6. Pregnant patients
    7. Breastfeeding women
  • Inability to provide informed consent

  • Any other factor that in the investigators' judgment may affect patient safety or compliance (e.g. distance greater than 100 miles from clinic).

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

49 participants in 2 patient groups, including a placebo group

Nitrous Oxide
Experimental group
Description:
One hour inhalation of nitrous oxide
Treatment:
Drug: Nitrous Oxide
Device: MRI
Placebo Gas
Placebo Comparator group
Description:
One hour inhalation of placebo gas
Treatment:
Drug: Placebo gas
Device: MRI

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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