Hypnosis may ease pain of hand injections, study finds
NCT ID NCT04328623
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether a short hypnosis session before an ultrasound-guided hand injection could lower pain. Eighty adults received either hypnosis or standard care. Researchers measured pain using a visual scale to see if the 'magic glove' technique helps.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- hypnosis
- What this could lead to
- If it works, this could offer a simple, drug-free way to reduce pain during hand injections.
- What could go wrong
- This is a small, completed study with only 80 people. The hypnosis technique may not work for everyone or in other settings.
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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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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80 people
The number who actually took part.
- Started
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Oct 2020
- Finished
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Sep 2022
- 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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18 years and older
- 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: * Patient with an indication of a first hand infiltration under ultrasound examination * Major patient * Patient with capacity to understand the protocol and has given oral consent to participate in the research, * Patient with social security coverage. Exclusion Criteria: * Patient having preventively applied a pain patch to the area to be infiltrated * Contraindication to infiltrations ( imbalanced diabetes, imbalanced,hypertension, ongoing infections). * Hearing impaired patient * Patient under guardianship/curtel * Minor * Pregnant woman * Patient participating in another intervention research protocol * Patient unable to follow the protocol as judged by the investigator.
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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
-
CHD Vendée
La Roche-sur-Yon, France, France
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