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临床试验/NCT00790179
NCT00790179已完成不适用

Continuous Lumbar Plexus Block for Postoperative Pain Control After Total Hip Arthroplasty

Northwell Health0 个研究点目标入组 225 人开始时间: 2003年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
225
主要终点
VAS pain scores

研究概览

简要总结

Continuous lumbar plexus and femoral blocks have been demonstrated to provide effective postoperative analgesia of the lower extremity following total joint arthroplasty. The purpose of this study was to compare these two techniques when used with intravenous patient-controlled analgesia and the use of patient-controlled analgesia alone for postoperative pain management following unilateral total hip arthroplasty.

详细描述

above may be applied

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 18-80 years old
  • primary diagnosis of osteoarthritis

排除标准

  • allergy to local anesthetics
  • peripheral neuropathy
  • opioid dependency
  • coagulopathy

结局指标

主要结局

VAS pain scores

时间窗: at 24 and 48 hours

次要结局

  • hydromorphone consumption,patient satisfaction,distance ambulated, opioid-related side effects(at 24 and 48 hours)

研究者

申办方类型
Other

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