Nitrous Oxide for the Treatment of Major Depressive Disorder

Last updated: December 10, 2024
Sponsor: Bayside Health
Overall Status: Completed

Phase

2

Condition

Depression (Adult And Geriatric)

Depression

Mood Disorders

Treatment

Placebo

Nitrous Oxide

Clinical Study ID

NCT03869736
438/19
  • Ages > 18
  • All Genders

Study Summary

The investigators are conducting a randomized controlled trial to evaluate the antidepressant effects of nitrous oxide in people with Major Depressive Disorder (MDD). MDD is a global medical condition that causes significant health and economic burden. Recent studies have shown that a single dose of ketamine, an NMDA-antagonist, has fast and long lasting anti-depressant effect. Nitrous oxide, another NMDA-antagonist, is widely used for anesthesia and analgesia, safer to administer and has fewer side effects than ketamine.

A randomized controlled crossover feasibility study showed significant reduction in depressive symptoms at 2 and 24 hours after a single 1-hour treatment session of inhaled nitrous oxide compared with placebo. Nitrous oxide is inexpensive and can be safely administered by any trained clinician. If found to be efficacious, it could be used to provide rapid anti-depressant effect whilst the benefit of traditional anti-depressants has its delayed effect. Another potential application could be in acutely suicidal patients.

This investigated-initiated phase 2b trial will enable confirmation and extension of the findings from the feasibility study, and identify the optimal dose and regimen in a broader population of those with MDD. Participants will be randomized to receive a weekly 1-hour inhalational sessions of either nitrous oxide or placebo (oxygen-air mixture) for 4 weeks, and the nitrous group will be further randomly assigned to a dose of 50% nitrous oxide or 25% nitrous oxide. Depression severity will be assessed by a blinded observer pre-treatment and at weekly intervals during and for 4 weeks after treatment using the Hamilton Depression Rating Scale.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Adult (≥18 years, both sexes), with DSM-IV-TR criteria for MDD without psychosis, asdetermined using a structured clinical interview [Mini InternationalNeuropsychiatric Interview]

  2. MDD, as defined by a pretreatment score >18 on the HDRS-21 scale

Exclusion

Exclusion Criteria:

  1. A history of bipolar disorder, schizophrenia, schizoaffective disorder,obsessive-compulsive disorder, panic disorder, or documented Axis II diagnoses;active suicidal intention, as determined by clinical interview

  2. Active or recent (<12 months) substance abuse or dependence; excluding nicotine

  3. Administration of NMDA-antagonists (e.g., ketamine) in previous 3 months

  4. Ongoing treatment with ECT

  5. Presence of acute medical illness that could interfere with study participation,including significant pulmonary disease

  6. Pregnancy or breastfeeding

  7. Any contraindications to the use of nitrous oxide (e.g., pneumothorax, middle earocclusion, elevated intracranial pressure, chronic cobalamin or folate deficiencyunless treated with folic acid or vitamin B12).

Study Design

Total Participants: 81
Treatment Group(s): 2
Primary Treatment: Placebo
Phase: 2
Study Start date:
January 22, 2019
Estimated Completion Date:
December 10, 2023

Connect with a study center

  • Alfred Hospital

    Melbourne, Victoria 3004
    Australia

    Site Not Available

  • University of Chicago Medicine

    Chicago, Illinois 60637
    United States

    Site Not Available

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