Efficacy and Safety of K-rod Dynamic Stabilization System in the Repair of Lumbar Degenerative Diseases
Study Details
Study Description
Brief Summary
To conduct a prospective, single-center, self-controlled, clinical trial to verify the efficacy and safety of K-Rod dynamic stability system in the repair of lumbar degenerative diseases following 2 years follow-up, aiming to provide references for clinical treatment of lumbar degenerative diseases.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
Posterior internal fixation and fusion systems are still one of the main methods for the treatment of chronic back pain due to intervertebral disc degeneration, but adverse reactions, such as accelerated regression of adjacent segments, are often inevitable during the treatment.
At present, various pedicle screw-based posterior dynamic stability systems of the lumbar spine have become an alternative fusion therapy for lumbar degenerative diseases. Dynamic stability is defined to reduce the loading on the intervertebral disc/articular surfaces, to maintain movement under mechanical load, to limit the abnormal movement of the spinal segment, and to reduce the stress on the bone-screw interface dynamically and stably. An ideal fixation system will be stable enough to maximize the fusion rate without the need for excessive rigidity, as well as to maintain maximum load and physiological posture of the vertebral segment, thereby reducing the horizontal stress of the adjacent segment.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: trial group Sixty-seven patients with lumbar degenerative diseases were treated with K-rod dynamic stabilization system. All patients were followed for 2 years. |
Device: K-rod dynamic stabilization system
Sixty-seven patients with lumbar degenerative diseases were treated with K-rod dynamic stabilization system. All patients were followed for 2 years. K-rod dynamic stabilization system was purchased from Biotech, USA, consisting of titanium alloy pedicle screw, titanium alloy line and polyether ether ketone (PEEK) shell between pedicle screw heads.
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Outcome Measures
Primary Outcome Measures
- Oswestry dysfunction index scores [at month 24 after surgery]
To quantify disability for pain. The Oswestry Disability Index questionnaire contains ten questions concerning intensity of pain, ability to take care of oneself, lifting, ability to walk, ability to sit, ability to stand, sleep quality, sexual life, social life, and ability to travel. Each question is scored on a scale of 0-5 with the first statement being zero and indicating the least amount of disability and the last statement is scored 5 indicating most severe disability.
Secondary Outcome Measures
- Lumbar lordosis angle [at month 24 after surgery]
The lumbar lordosis angle refers to an angle between the lower end plate of L1 and the upper end plate of S1 on the lateral X-ray.
Eligibility Criteria
Criteria
Inclusion Criteria:
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Degenerative lumbar spondylolisthesis (degree I)
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Nerve root canal or central spinal canal stenosis
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Accompanying nerve root pain and/or chronic back pain
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32-76 years old
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Regardless of gender
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All patients or family members signed the informed consent
Exclusion Criteria:
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Systemic infection;
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Poor compliance and inability to complete the trial
Contacts and Locations
Locations
No locations specified.Sponsors and Collaborators
- Shenyang Orthopedic Hospital
Investigators
- Principal Investigator: Shuyi Gong, Shenyang Orthopedic Hospital
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- ShenyangOrthoH-01