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Neck implant under review: does it ease pain and improve mobility?

NCT ID NCT07556978

Disease control Sponsor: MT Ortho s.r.l. 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026 · Last updated Jul 29, 2026 · Updated 2 times

Summary

This study reviews past medical records of 33 adults who had neck surgery with a special implant called ITC CERVICAL. The goal is to see if the device safely reduces neck disability and pain, and helps the spine heal properly. Researchers will look at data from before surgery, right after, and at a 3-month checkup.

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

32 people

The number who actually took part.

Started

May 2026

Finished

Jul 2026

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

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 subjects involved are patients with cervical disc disease or symptomatic degenerative disc disease, stenosis, radiculopathy and/or spondylosis, treated with cervical cages, aged \>18 years

Ages

18 to 84 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: * The participant must be able to understand the nature, objectives, risks, and benefits of the study and provide free and informed consent, in accordance with current regulations. * Patients undergoing primary ACDF (Anterior Cervical Discectomy and Fusion) at two or three (contiguous) levels between C2 and C7 * Diagnosis of symptomatic degenerative disc disease, including: myelopathy, radiculopathy, myeloradiculopathy, stenosis, herniated nucleus pulposus, spondylosis, osteophyte complexes, and foraminal stenosis * Availability and reliability of the neurological examination and pre- and post-operative clinical and radiological data and medical history * Adults (\>18 years) treated between 2020 and 2024 Exclusion Criteria: * Patients undergoing primary ACDF on a single level between C2 and C7 * History of previous surgeries in the anatomical area of interest

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Conditions

The condition(s) this trial relates to.

cervical disk degenerative disorder Klippel-Feil syndrome

As listed by the trial registrant

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

Cervical disc degenerative disorder Cervical fusion

Contacts and locations

Locations

  • "Humanitas" Istituto Clinico Catanese S.p.a.

    Misterbianco, Catania, 95045, Italy

  • Istituto Ortopedico "Villa Salus" Innocenzo

    Melilli, Siracusa, 96010, Italy

More trials for these conditions

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