Inhalational nitrous oxide as a transdiagnostic approach for the treatment of suicidal ideation and suicidality in psychiatric inpatients: protocol for a double-blind randomised, controlled clinical single-centre trial.
Golo Kronenberg, Anna Bankwitz, Barbora Provaznikova, Mario Müller, Boris B. Quednow, Erich Seifritz, Sebastian Olbrich
BMJ Open July 16, 2025 DOI: 10.1136/bmjopen-2024-096825 (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Randomized controlled trial Placebo-controlled Double-blind Pilot study Peer reviewed |
|---|---|
| Sample size | 85 |
| Population | Psychiatric inpatients |
| Intervention | Nitrous oxide (N2O) |
| Dose | 50% N2O and 50% oxygen |
| Duration | 45-minute inhalation session; second inhalation 1 week after first; primary outcome measured day before and day after first inhalation |
| Measures | Beck Scale for Suicidal Ideation |
| Keywords | Clinical pharmacology Psychometrics Suicide & self-harm |
| Registration | NCT06636357 |
| Key findings | The protocol tests whether inhalational N2O exerts rapid antisuicidal effects as a transdiagnostic treatment for suicidal ideation. |
Abstract
Suicidal thoughts and behaviours are linked to a wide range of mental health conditions. New interest in the psychiatric benefits of nitrous oxide (N2O) has only recently emerged. The broad pharmacological effects of N2O are thought to be due in large part to N-methyl-d-aspartate antagonism and opioid effects. The purpose of this study protocol is to test whether inhalational N2O exerts rapid antisuicidal effects as a transdiagnostic treatment for suicidal ideation. This is the protocol of a single-centre pilot study of N2O inhalation in 85 psychiatric inpatients. The initial 45-min double-blind, randomised, placebo-controlled inhalation session either consists of 50% N2O and 50% oxygen ('active treatment') or 50% oxygen plus air. The primary outcome is the change in Beck Scale for Suicidal Ideation scores between the day before and the day after inhalation. A second inhalation containing N2O will be administered 1 week after the first inhalation to ensure that all study participants receive the active treatment at least once. For the mechanism of action and prediction, a nested biomarker substudy will employ multimodal techniques, including analysis of hair and blood samples and electroencephalography. This study was approved by the local ethics committee ('Kantonale Ethikkommission-Kanton Zürich') and by the Swiss Agency for Therapeutic Products (Swissmedic). Study results will be disseminated primarily by peer-reviewed scientific journals and also by conference presentations, patient and public events and social media. ClinicalTrials.gov ID NCT06636357.
Citations in the library
Cites 12
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- Nitrous oxide as an adjunctive therapy in major depressive disorder: a randomized controlled double-blind pilot trial Brazilian Journal of Psychiatry February 18, 2021
- Pharmacological modelling of dissociation and psychosis: an evaluation of the Clinician Administered Dissociative States Scale and Psychotomimetic States Inventory during nitrous oxide (‘laughing gas’)-induced anomalous states Psychopharmacology March 26, 2022
- The boon and bane of nitrous oxide. European Archives of Psychiatry and Clinical Neuroscience September 1, 2025
- An Episode of Psychosis After Nitrous Oxide Abuse During a Pandemic: A Case Report. Cureus May 1, 2024
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