Hypnosis may help kids avoid pain gas during stitches

NCT ID NCT02420002

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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 Results may not be published yet.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)

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Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
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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.

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Status unknown
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First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 2 times

Summary

This study tested whether hypnosis, with MEOPA (a pain-relieving gas) available if needed, works as well as MEOPA alone for controlling pain in children getting stitches. Sixty children in the emergency department were randomly assigned to one of two groups. The goal was to see if hypnosis could reduce the need for MEOPA while still keeping kids comfortable.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
MEOPA (equimolar mixture of nitrous oxide and oxygen) and hypnosis
What this could lead to
If successful, this could show that hypnosis reduces the need for pain medication during minor procedures in children.
What could go wrong
This is a small, single-center trial with only 60 participants, so results may not apply broadly. Hypnosis may not work for all children, and some may still need MEOPA.

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

Phase 4

Runs after approval, following long-term safety and how well the treatment works in everyday use.

Participants

About 60 people

The number the study aims to enrol. It can still change while the study runs.

Started

Oct 2016

Finished

Mar 2025

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

4 to 17 years

Sex

Anyone

Healthy volunteers

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * The patient was informed about the implementation of the study, its objectives, constraints and patient rights * The legal representative of the patient must have given free and informed consent and signed the consent * The patient must be affiliated with or beneficiary of a health insurance plan * The patient is available for 15 days of follow-up * The patient is consulting in the emergency department for a wound requiring the completion of a suture and for which the operator considers that the use of nitrous oxide is necessary and possible. Exclusion Criteria: * The patient is participating in another interventional study * The patient has participated in another interventional study in the last 3 months * The patient is in an exclusion period determined by a previous study * The patient and/or his/her parents (or legal representative) refuses to sign the consent * It proves impossible to correctly inform the patient and / or his/her parents (or legal representative) * The patient has a contra-indication (or an incompatible drug combination) for a treatment required in this study (MEOPA): intracranial hypertension, impaired consciousness, pneumothorax, high rate oxygen-dependence, facial trauma preventing mask application. * The patient has a condition that makes hypnosis impossible: e.g. encephalopathy, deafness, communication disorders, does not speak French * Suture requiring surgical exploration or an operating room, or general anesthesia or an ears-nose-throat, orthopedic or visceral surgeon (e.g. wound of the oral cavity, abdominal or thoracic penetrating wound, finger or palm wound requiring exploration by an orthopaedist) * Fractures associated with wound * Use of level II/III analgesics before the beginning of pre-suture care support

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Conditions

The condition(s) this trial relates to.

injury Wounds, Nonpenetrating

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • CHRU de Nîmes - Hôpital Universitaire Carémeau

    Nîmes, 30029, France