Laughing gas may reveal brain clues for depression

NCT ID NCT04199143

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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

30 people

The number who actually took part.

Started

Feb 2020

Finished

Jun 2021

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

25 to 50 years

Sex

Female participants only

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show 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.

Depressive Disorder, Treatment-Resistant

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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