跳至主要内容
临床试验/jRCT1031210580
jRCT1031210580已完成不适用

Efficacy of intraoperative Nitrous Oxide use on postoperative pain in patients with cervical spinal cord injury: a randomized controlled trial

未提供0 个研究点目标入组 80 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
80
主要终点
-

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomized Controlled Trial
干预模型
Parallel Assignment
主要目的
Prevention Purpose
盲法
Double Blind

入排标准

年龄范围
20age old over 至 No limit(—)
性别
All

入选标准

  • Patients aged 20 years or older with ASIA classification C or D cervical spinal cord injury who underwent urgent spinal surgery

排除标准

  • Pneumothorax , head injury, limb injury : fracture/nerve injury, non-speaking Japanese, impaired consciousness ,Complications of psychiatric disorders :such as suicidal ideation, complications of other trauma, history of blood disorders

结局指标

主要结局

-

Pain intensity:NRS for the past 24 hours before and after surgery

次要结局

  • Changes in the range of postoperative neuropathic pain(1D, 2W, 3M, 6M)
  • Properties and intensity of neuropathic pain in the past 24 hours(1D, 2W, 3M, 6M)
  • Psychological state(2W, 3M, 6M)
  • ADL(2W, 3M, 6M)
  • Degree of improvement(2W, 3M, 6M)

研究者

发起方
未提供

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