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Spine surgery showdown: which procedure wins for neck stenosis?

NCT ID NCT07177651

Disease control Sponsor: Assiut University 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 This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Updated 1 time

Summary

This study compares two types of back surgery for people with narrowing of the spine in the neck (cervical stenosis). The goal is to see which surgery better improves nerve function and quality of life. Only 2 adults aged 40 and older who need surgery will take part, and they will be followed for 6 months.

What this could mean

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

Active substance
surgery (laminoplasty or laminectomy with lateral mass fixation)
What this could lead to
If successful, this could show which surgical approach is better for relieving nerve pressure and improving function in people with cervical spinal stenosis.
What could go wrong
This is a very small, early study with only 2 participants, so results may not apply to everyone. Both surgeries carry risks like infection or nerve damage.

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

About 2 people

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

Expected to start

Oct 2025

An estimate. Start dates often move.

Expected to finish

Mar 2027

An estimate. End dates often move.

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

40 years and older

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: * Patients aged 40 ≥ years with clinically significant cervical canal stenosis (based on imaging and neurological symptoms). * Surgical indication for cervical decompression. * Adequate follow up data (minimum 1 year). * Patients fit for surgery. Exclusion Criteria: * Patients unfit for surgery or contraindication to general anaesthesia. * Congenital deformities or significant spinal deformities unrelated to stenosis. * Patients with cervical kyphosis, active infection or known allergy to titanium. * Previous cervical spine surgery.

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Conditions

The condition(s) this trial relates to.

spinal stenosis

As listed by the trial registrant

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

Cervical stenosis Degenerative cervical spinal stenosis

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  2. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

More trials for these conditions

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