Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Cure My Disease

Don't miss your cure!

 Log in / Sign up

Standing within hours of spine surgery: a new test for teen recovery

NCT ID NCT06152601

Symptom relief Sponsor: University Hospital, Toulouse Source: ClinicalTrials.gov ↗

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 13, 2026 · Last updated Aug 14, 2026 · Updated 1 time

Summary

This trial tests whether children and teenagers who have just had surgery for idiopathic scoliosis can safely stand up within 6 hours after the operation. Participants will be helped by a physiotherapist to stand in an upright position, as part of an enhanced recovery program. The goal is to see if this early standing is feasible and how it affects pain and recovery.

What this could mean

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

Active substance
Early standing (bipedal standing position) within 6 hours after surgery, guided by a physiotherapist
What this could lead to
If early standing is feasible, it could help young patients recover faster and with less pain after scoliosis surgery.
What could go wrong
This is a small feasibility study, so success is not guaranteed. Standing too soon after major spine surgery may cause pain, dizziness, or other complications.

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

30 people

The number who actually took part.

Started

Mar 2024

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

12 to 18 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: * Programming of spinal surgery via the posterior approach for idiopathic scoliosis eligible for an ERAS program * Person affiliated or beneficiary of a social security scheme * Free, informed and written consent signed by the legal guardians of the minor patient * Free and informed consent of the minor patient Exclusion Criteria: * Scoliosis linked to a neuromuscular pathology * Physical status score of American Society of Anesthesiologists (ASA) \> 2 * Severe or unbalanced associated conditions (cardiac, pulmonary, coagulopathy or anticoagulant treatment with curative intent, long-term corticosteroid therapy) * Malnutrition * Major cognitive disorders * Impossibility for the parent(s) to contact the pediatrician or the hospital service if necessary (minor patients) * Pregnancy * Feeding with milk * Severe disability related to scoliosis with impossibility of ambulation * Surgical assembly planned unstable or requiring the wearing of a corset * Refusal of minor patient or of the legal guardians of the minor patient * Patient under legal protection, guardianship or curatorship

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for ERAS are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

Conditions

The condition(s) this trial relates to.

idiopathic scoliosis

As listed by the trial registrant

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

ERAS Idiopathic scoliosis

Contacts and locations

Locations

  • CHU de TOULOUSE

    Toulouse, 31000, France

More trials for these conditions

Other studies related to the condition(s) this trial covers.