跳至主要内容
临床试验/NCT02495805
NCT02495805撤回不适用

Ultrasound-guided Continuous Proximal Adductor Canal Versus Continuous Femoral Nerve Block for Postoperative Pain Control and Rehabilitation Following Total Knee Arthroplasty

Yale University0 个研究点开始时间: 2015年9月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
撤回
主要终点
Motor effects

研究概览

简要总结

The purpose of the study is to compare continuous femoral nerve block with continuous proximal adductor canal block for postoperative pain control and rehabilitation.

详细描述

Patients meeting the criteria: American Society of Anesthesiologists (ASA) class I and II, that are scheduled for elective total knee arthroplasty, will be recruited into the study. Subjects will be randomized into 2 groups: those who will receive a continuous proximal adductor canal block (ACB) and those who will receive a continuous femoral nerve block (FNB).

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
Single (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
是

入选标准

  • •Patients with an American Society of Anesthesiologists Physical Status Classification System (ASA) score of 1 or 2 that are healthy without systemic disease or have mild systemic disease, respectively.
  • •The patient will need to be able to have decision-making capacity and ability to consent for the study.

排除标准

  • •Patients with an American Society of Anesthesiologists Physical Status Classification System (ASA) score greater than
  • •Patients unable to have decision-making capacity and ability to consent for the study.

研究组 & 干预措施

adductor canal block (ACB)

Active Comparator

Subjects randomized to this groups receive a continuous proximal adductor canal block (ACB) during surgery.

干预措施: Continuous proximal adductor canal block (Procedure)

femoral nerve block (FNB)

Active Comparator

Subjects randomized to this groups receive a continuous femoral nerve block (FNB) during surgery.

干预措施: Continuous femoral nerve block (Procedure)

结局指标

主要结局

Motor effects

时间窗: 24 hours (postoperatively)

Subjects' change in motor effects will be assessed as maximum voluntary isometric contraction (MVIC) in the quadriceps muscle.

次要结局

  • Pain score(24 hours (postoperatively))
  • Opioid consumption(24 hours (postoperatively))
  • Motor effects(On average between 6 and 8 hours postoperatively)
  • Pain score(On average between 6 and 8 hours postoperatively)
  • Opioid consumption(On average between 6 and 8 hours postoperatively)

研究者

申办方类型
Other
责任方
Sponsor

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