跳至主要内容
临床试验/NCT04306666
NCT04306666Unknown不适用

Early Rehabilitation After Hand or Wrist Ambulatory Surgery : How to Preserve Locomotion at Home Without Rebound Pain? Study Walant " Wide Awake Local Anesthesia No Tourniquet " Versus Axillary Brachial Plexus Block.

University Hospital, Montpellier1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2019年12月30日最近更新:
适应症

试验速览

阶段
不适用
入组人数
60
试验地点
1
主要终点
duration of analgesia

研究概览

简要总结

The purpose of this retrospective study is to compare the analgesic efficacy of Walant " Wide Awake Local Anesthesia No Tourniquet " with lidocaine and bupivacaine versus axillary brachial plexus block using mepivacaïne, both performed by anesthesiologists, after hand or wrist ambulatory surgery.

The main objective is to prove that Walant block improve pain relief at home measuring time to first analgesic request.

The secondary objectives are to compare maximal pain, consumption of supplementary analgesics, and the duratin of sensory block between groups.

详细描述

data will be collected on patient records and will be compared between groups of regional anesthesia.

Data will be :

  • time to first analgesic request
  • sensory block
  • rescue analgesia during the first 24 hours after surgery
  • maximal pain score during the first 24 hours after surgery
  • patient satisfaction of managing care

研究设计

研究类型
Observational
观察模型
Other
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

  • All adults patients scheduled for hand or wrist ambulatory surgery since 2016
  • Exclusion criteria:

排除标准

  • 未提供

结局指标

主要结局

duration of analgesia

时间窗: 24 hours

time to first rescue analgesic request (opioid)

次要结局

  • duration of sensory block(24 hours)
  • maximal pain score during the first 24 hours after surgery(24 hours)
  • total rescue analgesia amounts the first 24 hours after surgery(24 hours)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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