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Can timing of spine surgery predict how well arm weakness recovers?

NCT ID NCT07825545

Knowledge-focused Sponsor: University Hospital of North Norway 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Sep 17, 2026 · Last updated Sep 18, 2026 · Updated 1 time

Summary

Researchers are studying people who have surgery for cervical radiculopathy, a condition where a pinched nerve in the neck causes arm or hand weakness. The study follows about 2,000 patients to see how many recover full strength and whether factors like how severe the weakness was or how long it lasted before surgery affect the outcome. Participants answer questions about their strength and neck-related disability at 3 and 12 months after their operation. The goal is to help doctors and patients make better decisions about when to operate and what to expect.

What this could mean

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

Active substance
cervical spine surgery (anterior disc removal and fusion, or posterior decompression)
What this could lead to
If the study clarifies how weakness severity and how long symptoms last affect recovery, doctors and patients could make better-informed choices about when to operate.
What could go wrong
This is an observational study, so it can show patterns but cannot prove that surgery causes better recovery. Results may not apply to people with different spine conditions or to those who do not have surgery.

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

2,000 people

The number who actually took part.

Started

Jan 2012

Finished

Dec 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.

Who is studied

The study will include consecutive patients operated for DCR and registered in NORspine form January 2012 through 2022, approximately 12.000 cases. Patients operated for cervical myelopathy will be excluded. Otherwise patients under the age of 16, those operated for fractures, tumours and primary infections, as well as those unable to give informed consent, are not included in the NORspine.

Ages

16 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: * Surgery due to degenerative cervical radiculopathy with a preoperative muscle weakness * Posterior and anterior approach (ACDF/artificial disc replacement, posterior foramenotomi) Exclusion Criteria: * Myelopathy as surgical indication * Tumor as surgical indication * Infection as surgical indication * Fracture as surgcial indication * Posterior fusion and laminectomy * Prior cervical surgery * Anterior corpectomy

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Conditions

The condition(s) this trial relates to.

cervical disk degenerative disorder Muscle Weakness spondylosis spondylosis, cervical

As listed by the trial registrant

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

Cervical disc herniation Cervical radicular pain Cervical spine disc disease Muscle weakness Spondylosis, cervical

Contacts and locations

Locations

  • Neurosurgical department, University Hospital of North Norway

    Tromsø, 9010, Norway

More trials for these conditions

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