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临床试验/JPRN-UMIN000008840
JPRN-UMIN000008840已完成3 期

Postoperative quadriceps strength of continuous femoral ropivacaine or levobupivacaine: a prospective, randomized double-blind trial after total knee arthroplasty - Postoperative quadriceps strength of continuous femoral ropivacaine or levobupivacaine: a prospective, randomized double-blind trial after total knee arthroplasty

Department of Anesthesia and Intensive Care Medicine, Osaka University Graduate School of Medicine0 个研究点目标入组 24 人开始时间: 2012年10月3日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
24

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1.Inability to communicate lucidly 2.Bilateral TKA 3.revision knee arthroplasty 4.Under 20 years old 5.Allergy to any of the drugs used in this study 6.ASA-PS > III 7.Chronic opioid use 8.Diabetes mellitus with sensory disorders 9.Neurological disability 10.Infections around femoral crease 11.Platelet < 5.0 * 10^4 /mcl 12.Pregnancy, possibility of pregnancy, or breast-feeding women 13.Contraindications to peripheral nerve blocks

研究者

发起方
Department of Anesthesia and Intensive Care Medicine, Osaka University Graduate School of Medicine

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