KCT0006191已完成未知
Evaluation of the efficacy and safety of conventional and minimally invasive biportal endoscopic spine surgery to treat herniated intervertebral disc: A prospective, Randomized, Assessor blind, Multicenter trial
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 100
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional Study
入排标准
- 年龄范围
- 20(Year) 至 80(Year)（—）
- 性别
- All
入选标准
- •1. 20~80 years of age at the date of written informed consent.
- •2. Patients who have unilateral or bilateral radiculopathy resulting from lumbar disc herniation and can be followed up for more than 1 year.
- •3. A person who voluntarily signed a written consent after hearing the explanation of the purpose and method of this clinical trial.
排除标准
- •1. Spondylolisthesis of Meyer Gr II or higher
- •2. Prior surgery at the same level
- •3. Lumbar degenerative scoliosis (Cobb angle>20)
- •4. In case of other spinal diseases in the affected area (ankylosing spondylitis, tumor, compression fracture, etc.)
- •5.Psychiatric illness (Dementia, mental illness)
- •6. Those who refused to participate in the study.
- •7. Others, if judged by the investigator to be inappropriate for participation in this clinical trial.
研究者
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