Laughing gas for depression? study pulled before start
NCT ID NCT05357040
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study aimed to see if nitrous oxide (laughing gas) could help people with major depression, especially those who hadn't improved with other treatments. Participants would have received four weekly sessions of the gas or a placebo. However, the study was withdrawn before any volunteers were enrolled.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Started
-
Jun 2021
- Finished
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Feb 2026
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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).
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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The Alfred Hospital
Melbourne, Victoria, 3004, Australia
-
University of Chicago Medicine
Chicago, Illinois, 60637, United States
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Other studies related to the condition(s) this trial covers.
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