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Spine surgery may improve posture in lumbar stenosis patients

NCT ID NCT03065452

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study looked at 72 people with lumbar stenosis who had decompression surgery to relieve leg and back pain. Researchers wanted to see if the surgery also improved their posture, specifically a forward-leaning stance. They used special X-ray imaging to measure changes in spine alignment and compared them to symptom reports. The goal was to learn more about how surgery affects both pain and posture.

What this could mean

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

Active substance
decompression surgery
What this could lead to
If successful, this could help doctors understand how spine surgery improves posture and guide better treatment for lumbar stenosis.
What could go wrong
This is a small, completed observational study, not a treatment trial. Results may not apply to all patients, and no new therapy is being tested.

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.

Participants

72 people

The number who actually took part.

Started

Nov 2014

Finished

May 2016

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.

Who is studied

consecutive patients who underwent open decompression surgery (laminotomy) were prospectively included in this study

Ages

Children (under 18), adults (18 to 64) and older adults (65 and over)

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: 1. Symptoms and signs of neurogenic claudication and radiological signs of central lumbar stenosis; 2. Patients undergoing open decompression surgery ≤ 3 levels, 3. All patients with symptoms that did not respond to at least 3 months of non-invasive treatment. Exclusion Criteria: Patients were excluded from the study if they had one or several of the following clinical and/or radiological criteria: 1. spondylolisthesis (disc slip \> 5 mm), 2. criteria showing instability (variation of \> 10° in the angle formed by the vertebral endplates on dynamic images). 3. scoliosis (Cobb angle \> 20 °). 4. Patients lost to follow-up were excluded.

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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

  • Chu de Dijon

    Dijon, 21079, France

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