KCT0005793
Completed
未知
Evaluation of the efficacy and safety of 3D printing porous titanium cage with Non-Window type versus Window type in lumbar interbody fusion: A prospective, randomized, multicenter trial
Chung-Ang Univerisity Hospital0 sites70 target enrollmentTBD
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Chung-Ang Univerisity Hospital
- Enrollment
- 70
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •? Patients with degenerative spinal diseases of the lumbar spine and need single\-segment interbody fusion because there is no symptom improvement even after conservative treatment for at least 6 weeks
- •? Patients with confirmed spinal degenerative diseases related to symptoms by X\-ray and MRI examination
- •? Patients with no communication problems in conducting and conducting clinical research
- •? Patients who participate in the test, observe treatment and procedures, and are willing to visit the hospital for all follow\-up evaluation
- •? Patients who voluntarily agree to participate in clinical research and are willing to comply with the subject matters
Exclusion Criteria
- •? Patients under 18 years of age or over 80 years of age
- •? Patients unable to perform spinal surgery under general anesthesia due to severe heart, lung disease, liver disease, and kidney function decline
- •? Patients scheduled for surgery due to spinal infection or tumor within 12 months from registration
- •? Those who take drugs that may affect bone union immediately before or after surgery (eg, steroids, parathyroid hormone, etc.)
- •? Patients whose remaining life expectancy is less than 1 year
- •? Patients in the age group who are pregnant and planning to become pregnant during the study period
- •? Patients who are not suitable for this clinical study in the opinion of the researcher or who may increase the risk associated with participation in the study
Outcomes
Primary Outcomes
Not specified
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