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临床试验/NCT02186795
NCT02186795已完成不适用

Improvement in Total Hip Arthroplasty Patient Outcomes With Regional Anesthesia and Multimodal Analgesia: A Retrospective Analysis

Medical University of South Carolina1 个研究点 分布在 1 个国家目标入组 117 人开始时间: 2013年4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
117
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 and administration of multimodal oral analgesia 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, assitstance 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

  • Primary total hip arthroplasty, (identified by current procedural terminology (CPT) code 27130) and
  • Either a) Epidural or b) Lumbar plexus peripheral nerve block with the administration of multimodal medication after July

排除标准

  • Exclusion criteria include THA Revision, ICU admission postoperatively, and dementia, not allowing pain score communication.

结局指标

主要结局

Opiate Consumption

时间窗: 48 hours postoperative

Cumulative 48 Hours Opiate Consumption in Intravenous (IV) Morphine mg Equivalents (MME)

次要结局

未报告次要终点

研究者

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

Sylvia Wilson

Assistant Professor

Medical University of South Carolina

研究点 (1)

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