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临床试验/KCT0009256
KCT0009256
尚未招募
未知

A prospective randomized controlled trial analyzing the clinical outcomes and patient satisfaction based on the implementation of the clinical pathway for Enhanced Recovery After Surgery program (ERAS CP) following oblique lumbar interbody fusion (OLIF)

Seoul National University Hospital0 个研究点目标入组 38 人待定

概览

阶段
未知
干预措施
未指定
疾病 / 适应症
未指定
发起方
Seoul National University Hospital
入组人数
38
状态
尚未招募
最后更新
2年前

概览

简要总结

暂无简介。

注册库
who.int
开始日期
待定
结束日期
待定
最后更新
2年前
研究类型
Interventional Study
性别
All

研究者

入排标准

入选标准

  • A. Patients who are able to ambulate independently for more than 30 minutes (see below for specific screening details):
  • i. Patients who, despite intermittent claudication, are able to reach a target distance of more than 30 minutes by taking breaks intermittently during ambulation are included.
  • ii. Patients who are able to reach a target distance of more than 30 minutes despite experiencing severe pain are also included.
  • B. Patients who visited the neurosurgery outpatient clinic for surgical treatment due to lumbar degenerative disease, requiring 1\-2 segmental fixation between lumbar 2 and sacral 1\.
  • C. Patients who voluntarily agree to participate in the research

排除标准

  • A. Patients who have previously undergone lumbar surgery.
  • B. Patients with muscle weakness of Manual Muscle Testing grade 3 or higher.
  • C. Patients with coexisting neuropsychiatric disorders, such as depression.
  • D. Patients with musculoskeletal diseases (inflammatory, myopathic, etc.) and infections other than lumbar degenerative disease.
  • E. Patients with concurrent malignant disease.
  • F. Patients who do not wish to participate in the research

结局指标

主要结局

未指定

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