VR hypnosis may replace laughing gas for scared kids at the dentist
NCT ID NCT05167331
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether virtual reality hypnosis can reduce anxiety and pain in children during dental procedures as effectively as nitrous oxide (laughing gas). Thirty anxious children aged 7 to 10 took part. Researchers measured their behavior and pain levels to compare the two approaches.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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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 2022
- Finished
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Nov 2024
- 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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7 to 10 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion criteria: * Patients aged between 7 and 10 years * With an indication for conservative and/or endodontic care of at least 2 temporary molars belonging to the same dental arch, unilateral or bilateral, and equivalent in terms of caries and symptoms * With dental anxiety * ASA I patients Exclusion criteria: * Patient with a history of MEOPA or virtual reality sedation for dental treatment * Patient refusing to do preoperative intra-oral x-rays * Patient with one of the MEOPA contraindications * Patient with a history of post-operative nausea vomiting or motion sickness * Patient with visual or hearing disorders * Patient presenting with a psychiatric pathology or having taken psychotropic drugs in the 8 weeks preceding the 1st visit and during the duration of the study * Patient with claustrophobia * Patient without French Social Security coverage * Lack of consent from the holders of parental authority to participate in the study
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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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Les Hôpitaux Universitaires de Strasbourg
Strasbourg, 67091, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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