跳至主要内容
临床试验/KCT0005938
KCT0005938尚未招募未知

Intraoperative Fluoroscopic-guided Erector Spinae Plane Block in Oblique Lumbar Interbody Fusion Surgery

POHANG STROKE AND SPINE HOSPITA0 个研究点目标入组 40 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
40

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 75(Year)(—)
性别
All

入选标准

  • Patients performing one spinal level OLIF surgery.
  • age 20 to 75 years old
  • American Society of Anesthesiologists (ASA) physical status of 1–3

排除标准

  • Previous spinal surgery
  • Bleeding tendency or anticoagulation
  • Allergic reaction to the contrast agent
  • Allergic reaction to the local anesthetic agent
  • Chronic usage of narcotic painkillers
  • Functional conditions that are unable to walk due to paralysis of the lower extremities
  • Impossible to assess pain due to communication difficulties
  • If the patient refuses or does not agree to participate
  • Severe liver disease, kidney disease, arrhythmia patients (risks for using ropivacaine)

研究者

发起方
POHANG STROKE AND SPINE HOSPITA

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