Could a 10-Minute gas fix autism social struggles?
NCT ID NCT07435103
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This early study tests whether inhaling a gas called xenon for 10 minutes a day over 10 days can improve social functioning in children with autism. 72 children aged 4-18 will receive either xenon or a placebo. Researchers will check social skills right after treatment and again 3 months later.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- xenon gas
- What this could lead to
- If it works, this could point toward a new, short-term treatment to ease social difficulties in children with autism.
- What could go wrong
- This is a very early, small trial (Phase 1/2) with only 72 children. The effect may be small or absent, and long-term safety is unknown.
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 1/2
Runs two stages together: safety and dose first, then whether the treatment works.
- Participants
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About 72 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Mar 2026
An estimate. Start dates often move.
- Expected to finish
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Jun 2027
An estimate. End dates often move.
- 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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4 to 18 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: * Aged 4-18 years, with no gender restriction. * Meeting the diagnostic criteria for Autism Spectrum Disorder (ASD) as specified in the Diagnostic and Statistical Manual of Mental Disorders (5th Edition) (DSM-5), with the diagnosis confirmed by assessment using the Autism Diagnostic Observation Schedule, Second Edition (ADOS-2). * The total T-score on the Social Responsiveness Scale, Second Edition (SRS-2) is ≥90. * No treatment such as neuromodulation (transcranial magnetic stimulation, transcranial electrical stimulation) has been received for at least 1 month prior to randomization. * For participants who have previously taken psychotropic medications prior to randomization, it is required that the medications have been discontinued for a minimum of 5 half-lives or 4 weeks, whichever is longer. * The participants and their legal guardians confirm that they will not add new or alter the existing established treatment regimens such as behavioral rehabilitation during the study period. * The legal guardians of the participants have a full understanding of the study content, participate voluntarily, and sign a written informed consent form. Exclusion Criteria: * Having other major neurological diseases (e.g., epilepsy, cerebral palsy), severe physical illnesses, or genetic syndromes. * Having severe auditory or visual impairments that prevent the completion of assessments with cooperation. * A history of anaphylaxis or adverse reactions to Xenon. * Currently participating in or having participated in other interventional clinical trials within the recent 3 months. * The investigator judges that there is any condition that may increase the risk to the participant or interfere with the conduct of the trial and the assessment of its results.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Children's Hospital Affiliated to Zhejiang University School of Medicine (Binjiang Campus)
Hangzhou, Zhejiang, 310000, China
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- Can visual cues unlock sentence building in children with language delays?