Laughing gas may reveal brain clues for depression
NCT ID NCT04199143
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study looks at how nitrous oxide (laughing gas) changes brain activity in people with treatment-resistant depression. Researchers used ultrasound and MRI to measure brain blood flow and connectivity before, during, and after a one-hour dose of the gas. The goal is to find brain markers that could predict who will respond to this potential treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Nitrous oxide (laughing gas) mixed with oxygen
- What this could lead to
- If successful, this could help identify which patients with treatment-resistant depression might benefit from nitrous oxide therapy, leading to more personalized treatment.
- What could go wrong
- This is a small pilot study with only 30 participants, so results may not apply broadly. It focuses on brain imaging changes, not on proving antidepressant effectiveness.
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
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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30 people
The number who actually took part.
- Started
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Feb 2020
- Finished
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Jun 2021
- Lead sponsor
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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
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25 to 50 years
- Sex
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Female participants only
- Healthy volunteers
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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: * Inclusion criteria common to all participants * Female between 25 and 50 years of age * A person who can undergo N2O diffusion via a facial mask. * A person who has signed an informed consent. * Person affiliated with a social security scheme. * Inclusion Criteria for Depressive Patients * Major Depressive Episode according to DSM-5 criteria, confirmed by the MINI - International Neuropsychiatric Interview. * Patients with an MADRS score greater than 20 (Montgomery * Asberg Depression Rating Scale). * Patients resistant to at least one well-conducted antidepressant treatment, as documented by the MGH-ATRQ scale. * Absence of: bipolar disorder, schizophrenic disorder, neurodegenerative disease, schizophrenic disorder, neurodegenerative disease, addiction to one or more toxics documented by the MINI. * Inclusion criteria for healthy voluntary controls * Absence of: bipolar disorder, schizophrenic disorder, neurodegenerative disease, schizophrenic disorder, neurodegenerative disease, addiction to one or more toxics documented by the MINI, current or past. Exclusion Criteria: * Unstable somatic pathology (including unstable neurological or cardiological pathologies at risk of interfering with N2O diffusion) * Presence of active and significant psychotic symptoms, at investigator's discretion * Contraindications to mixture 50%N2O/ 50%O2: intracranial hypertension, altered state of consciousness, head trauma, pneumothorax, emphysema bubbles, abdominal gaseous distension, administration of less than 3 months of ophthalmic gas (SF6, C3F8,C2F6) used in eye surgery, known and unsubstituted deficiency in vitamin B12 or folic acid, recent and unexplained neurological abnormalities. * Contraindications to MRI, including claustrophobia. * Female who is pregnant or breastfeeding or able to procreate without an effective contraceptive method * Legal incapacity and/or other circumstances rendering the patient unable to understand the nature, purpose or consequences of the study (including major under legal protection). * A person participating in a drug clinical trial or during a period of exclusion from any clinical study due to previous involvement.
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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
-
University Hospital of Tours
Tours, 37044, France
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Other studies related to the condition(s) this trial covers.
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