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临床试验/NCT02493621
NCT02493621已完成不适用

Compare Effectiveness of Epidural vs. Lumbar Plexus Blocks in Total Hip Arthroplasty (THA) Patients Using Multimodal Pain Control

Medical University of South Carolina1 个研究点 分布在 1 个国家目标入组 116 人开始时间: 2014年12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
116
试验地点
1
主要终点
Opiate Consumption

研究概览

简要总结

The goal of this retrospective chart review is to evaluate if the implementation of lumbar plexus block placement for postoperative pain have improved conditions in the postoperative period for patients undergoing total hip arthroplasty when compared to the placement of epidurals for postoperative pain management.

详细描述

Primary outcome: 48 hour opiate consumption in patients following THA. ' Secondary outcome: Time to first ambulation, assistance needed with ambulation, opiate and regional related side effects, time to discharge orders.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Retrospective

入排标准

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

入选标准

  • 18 years and older
  • Diagnosis of:
  • Primary THA, (identified by CPT code 27130)
  • Either a) Epidural (CPT code 62319) or b) Lumbar plexus peripheral nerve block (CPT 62311 or 64449)
  • Perioperative multimodal medication
  • Hospitalized from July 1, 2012 to December 17, 2014.

排除标准

  • THA Revision
  • ICU admission postoperatively
  • History of dementia

结局指标

主要结局

Opiate Consumption

时间窗: 48 hours postoperative

Cumulative opiate consumption in intravenous (IV) morphine mg equivalents (MME)

次要结局

  • Time of First Ambulation(48 hours)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Sylvia Wilson

Associate Professor

Medical University of South Carolina

研究点 (1)

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