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Virtual reality training could make spinal taps safer for patients

NCT ID NCT05269238

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 1 time

Summary

This study looked at whether training with an augmented reality simulator helps medical students perform lumbar punctures (spinal taps) better than standard teaching. Lumbar punctures can be stressful for both patients and doctors. The simulator uses haptic feedback to mimic the feel of the procedure. 60 patients who needed a lumbar puncture took part, and researchers compared success rates between students trained with the simulator and those trained the usual way.

What this could mean

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

What this could lead to
If successful, this could lead to better training methods for doctors, reducing patient discomfort and improving success rates for lumbar punctures.
What could go wrong
This is a small, completed study focused on training, not a treatment. Results may not apply to all medical procedures or 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

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

60 people

The number who actually took part.

Started

Dec 2021

Finished

Nov 2023

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

18 years and older

Sex

Anyone

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: * Requiring a lumbar puncture as part of their routine care * Male or female of legal age with no upper age limit * French speaking * Subject affiliated to a social health insurance scheme * Not having expressed his or her opposition to the re-use of his or her data in the context of this research Exclusion criteria: * Previously undergone a lumbar puncture * BMI \> 35 kg/m². * Spinal ankylosis: history of ankylosing spondylitis or Forestier's disease * Impossible to give the subject informed information (subject in an emergency situation, difficulties in understanding the subject, etc.) * Subject under court protection * Subject under guardianship or curatorship * Contraindication to the use of Emlapatch

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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

  • Hôpitaux Universitaires de Strasbourg

    Strasbourg, 67091, France

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