Minimally Invasive Posterior Decompression of the Cervical Spine (NCT06995300) | Clinical Trial Compass
RecruitingNot Applicable
Minimally Invasive Posterior Decompression of the Cervical Spine
Russia30 participantsStarted 2025-05-19
Plain-language summary
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.
Who can participate
Age range18 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria
✓. Over 18 years old;
✓. Degenerative symptomatic cervical stenosis caused by posterior compression (hypertrophied ligament flavum and/or hypertrophied facet joints etc.) confirmed by MRI;
✓. Symptoms persisting for at least 3 months prior to surgery;
✓. Planned surgical decompression for one and more cervical level;
✓. Given written Informed Consent;
✓. Able and agree to fully comply with the clinical protocol and willing to adhere to follow-up schedule and requirements.
Exclusion criteria
✕. The need for anterior cervical decompression;
✕. Prior cervical fusion at any level;
✕. Any contraindication or inability to undergo baseline and/or follow up MRI or X-ray as required per protocol;
✕. Neck or non-radicular pain of unknown etiology;
What they're measuring
1
Change in the cross-sectional area of the dural sac, mm2
Timeframe: 3 months after surgery
Trial details
NCT IDNCT06995300
SponsorN.N. Priorov National Medical Research Center of Traumatology and Orthopedics