Image

Minimally Invasive Posterior Decompression of the Cervical Spine

Minimally Invasive Posterior Decompression of the Cervical Spine

Recruiting
18 years and older
All
Phase N/A

Powered by AI

Overview

Degenerative stenosis of the cervical spinal canal may be caused by the compression of the posterior part of the dural sac and spinal cord by the hypertrophied ligamentum flavum and facet joints, by the compression of the anterior part of the dural sac and spinal cord by the posterior longitudinal ligament, vertebral osteophytes and protrusion/ herniation.

The choice of surgical treatment in such cases is challenging. Posterior decompression and fixation is often proposed, but it is associated with a traumatic posterior approach, a large wound, and blood loss, a high risk of surgery site infections, and also instability of the metal fixation is possible. Also important is the increase in the surgical procedure cost due to the use of metal implants. An excellent alternative to standard posterior decompression and fixation is a method with isolated decompression of the cervical canal via posterior approach, which does not require any metal fixation.

Eligibility

Inclusion Criteria:

  1. Over 18 years old;
  2. Degenerative symptomatic cervical stenosis caused by posterior compression (hypertrophied ligament flavum and/or hypertrophied facet joints etc.) confirmed by MRI;
  3. Symptoms persisting for at least 3 months prior to surgery;
  4. Planned surgical decompression for one and more cervical level;
  5. Given written Informed Consent;
  6. Able and agree to fully comply with the clinical protocol and willing to adhere to follow-up schedule and requirements.

Exclusion Criteria:

  1. The need for anterior cervical decompression;
  2. Prior cervical fusion at any level;
  3. Any contraindication or inability to undergo baseline and/or follow up MRI or X-ray as required per protocol;
  4. Neck or non-radicular pain of unknown etiology;
  5. History or presence of any other major neurological disease or condition that may interfere with the study assessments;
  6. Previous enrollment in this study, current enrollment or plans to be enrolled in another study (in parallel to this study).

Study details
    Cervical Degenerative Disc Disease
    Cervical Stenosis
    Posterior Spine Surgery

NCT06995300

N.N. Priorov National Medical Research Center of Traumatology and Orthopedics

15 October 2025

Step 1 Get in touch with the nearest study center
We have submitted the contact information you provided to the research team at {{SITE_NAME}}. A copy of the message has been sent to your email for your records.
Would you like to be notified about other trials? Sign up for Patient Notification Services.
Sign up

Send a message

Enter your contact details to connect with study team

Investigator Avatar

Primary Contact

  Other languages supported:

First name*
Last name*
Email*
Phone number*
Other language

FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.