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临床试验/NCT02289937
NCT02289937已完成4 期

Effect of a Lateral Nerve of the Thigh Block on Postoperative Pain After Total Hip Replacement Surgery: a Clinical Randomized Trial

Daniel Hägi-Pedersen0 个研究点目标入组 100 人开始时间: 2014年3月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
100
主要终点
VAS-score 4 hours postoperative during movement

研究概览

简要总结

The purpose of this study was to evaluate the analgesic efficacy of the nervus cutaneous femoral lateralis (NCFL) blockade on postoperative pain after total hip replacement surgery. The NCFL-block is a pure sensory block. We hypothesized that the NCFL-block would reduced the postoperative pain without delaying mobilization.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

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 replacement

排除标准

  • general anaesthesia
  • Allergy to local anesthetics of the amide type
  • Revision surgery
  • Bilateral surgery
  • Chronic pain patient
  • Women in the fertile age

研究组 & 干预措施

Ropivacaine

Experimental

8 ml of ropivacaine 7,5 mg/ml will be injected around nervus cutaneous femoral lateralis. Ultrasound-guided.

干预措施: Ropivacaine (Drug)

Ropivacaine

Experimental

8 ml of ropivacaine 7,5 mg/ml will be injected around nervus cutaneous femoral lateralis. Ultrasound-guided.

干预措施: An ultrasound-guided Nervus cutaneous femoral lateralis blockade will be given postoperatively (Device)

Placebo

Placebo Comparator

8 ml of isotonic saline will be injected around nervus cutaneous femoral lateralis. Ultrasound-guided

干预措施: Placebo (Drug)

Placebo

Placebo Comparator

8 ml of isotonic saline will be injected around nervus cutaneous femoral lateralis. Ultrasound-guided

干预措施: An ultrasound-guided Nervus cutaneous femoral lateralis blockade will be given postoperatively (Device)

结局指标

主要结局

VAS-score 4 hours postoperative during movement

时间窗: 4 hours postoperative

VAS-score 4 hours postoperative during 30 degrees of flexion of the hip. VAS-score: 0-100 mm; 0: no pain, 100: worst imaginable pain.

次要结局

  • Oxynorm consumption(0-24 hours postoperative)
  • Mobilization(0-24 hours postoperatively)
  • Length of stay(0-7 days postoperative)
  • VAS-score 0-24 hours postoperative during movement(0-24 hours postoperatively)
  • VAS-score 0-24 hours postoperative at rest(0-24 hours postoperatively)
  • time to first oxynorm requirement(0-24 hours postoperatively)

研究者

发起方
Daniel Hägi-Pedersen
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Daniel Hägi-Pedersen

Consultant

Naestved Hospital

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