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Antidepressant Effects of Nitrous Oxide
NCT05357040 · University of Chicago
In plain English
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Official title
Evaluation of the Antidepressant Effects of Nitrous Oxide in People With Major Depressive Disorder
About this study
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 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 session 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% or 25% nitrous oxide. Depression severity and outcomes related to treatment responses will be continuously assessed by a 'blinded-to-randomization' psychiatry (MD) rater at weekly intervals during study patient participation, using validated psychiatric diagnostics (Hamilton Depression Rating Scale-21 \[HDRS-21 or HAM-D\]; Profile of Mood States \[POMS\]; Computerized Adaptive Test-Mental Health \[CAT-MH\]; Sheehan-STS \[S-STS\]; Visual Analog Scale \[VAS\]).
Eligibility criteria
Inclusion Criteria:
1. Adult (≥18 years, both sexes)
2. DSM-5 criteria for MDD without psychosis, as determined using a structured clinical interview \[Mini International Neuropsychiatric Interview\], MDD, defined by a pre-treatment score \>16 on the HDRS-21 scale and meeting DSM-5 for MDD
Exclusion Criteria:
1. A current or past history of bipolar disorder, schizophrenia, or schizoaffective disorder.
2. Current obsessive-compulsive disorder, panic disorder, or documented Axis II diagnoses
3. Active suicidal intention, as determined by clinical interview assessment tool (Sheehan-STS) and clinical examination
4. Active or recent (\<12 months) substance use disorder; excluding nicotine
5. Administration of NMDA-antagonists (e.g., ketamine) in previous 3 months
6. Ongoing treatment with ECT
7. Presence of acute medical illness that could interfere with study participation, including significant pulmonary disease
8. Pregnancy or breastfeeding
9. Any contraindications to the use of nitrous oxide (e.g., pneumothorax, middle ear occlusion, elevated intracranial pressure, chronic cobalamin or folate deficiency unless treated with folic acid or vitamin B12).
Study design
Enrollment target: 172 participants
Allocation: randomized
Masking: double
Age groups: adult, older_adult
Timeline
Starts: 2021-06-30
Estimated completion: 2026-12-01
Last updated: 2026-01-12
Interventions
Drug: Nitrous oxide gas for inhalationDrug: Placebo
Primary outcomes
- • Change in HDRS-21 score (Over 4-weeks from baseline)
Sponsor
University of Chicago · other
With: The Alfred
Contacts & investigators
ContactFrank Brown Jr · contact · fbrown@dacc.uchicago.edu · 773-834-5778
InvestigatorPeter Nagele, MD, MSc · principal_investigator, University of Chicago, Department of Anesthesia and Critical Care
InvestigatorPaul Myles, MD · principal_investigator, The Alfred Hospital, Department of Anesthesiology and Perioperative Medicine
All locations (2)
University of Chicago MedicineRecruiting
Chicago, Illinois, United States
The Alfred HospitalRecruiting
Melbourne, Victoria, Australia