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临床试验/NCT05390450
NCT05390450已完成不适用

Ultrasound-Guided Popliteal Plexus Block Versus Fascia Iliaca Block for Postoperative Analgesia After Total Knee Arthroplasty: A Randomized Clinical Trial

Tanta University2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2022年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
60
试验地点
2
主要终点
Total intravenous (IV) morphine consumption

研究概览

简要总结

This study aims to investigate the effect of the Popliteal Plexus Block versus Fascia Iliaca Block on postoperative pain after total knee arthroplasty.

详细描述

The Popliteal Plexus entwines the popliteal artery and vein contiguous to the adductor hiatus in the popliteal fossa and innervates the posterior capsule as well as intraarticular genicular structures. It was recently confirmed in a cadaver study that injection of 10 mL of dye into the distal end of the adductor canal spreads via the adductor hiatus to the popliteal fossa and stains the Popliteal Plexus.

Recently, fascia iliaca block was proposed as a popular analgesic technique which involves local infiltration anesthesia under the fascia of the iliacus muscle. The method depends on the local anesthetics spread beneath the fascia to block the peripheral nerve. It has been proposed to avoid the complications by anesthetizing the femoral nerve remotely from major neurovascular structures and achieve adequate analgesia.

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
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
40 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 40 - 75 years.
  • Both sexes.
  • American Society of Anesthesiologists (ASA) score I-II.
  • Scheduled for unilateral, primary TKA under spinal anesthesia.

排除标准

  • Coagulopathy.
  • Diabetes.
  • Heart failure.
  • kidney failure.
  • Liver failure.
  • Reduced sensation on the lower limb.
  • Daily intake of opioids.
  • Contraindication to any drug used in the study.

结局指标

主要结局

Total intravenous (IV) morphine consumption

时间窗: 24 hours postoperatively.

Total intravenous (IV) morphine consumption during the first postoperative 24 hours, postoperatively.

次要结局

  • First analgesic request(24 hours postoperatively)
  • Pain level score(24 hours postoperatively)
  • Patient's satisfaction level(24 hours postoperatively)
  • Rehabilitation(24 hours postoperatively)

研究者

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

Taysser Mahmoud Abdalraheem

Lecturer of Anesthesiology, Surgical Intensive Care and Pain Medicine, Faculty of Medicine

Tanta University

研究点 (2)

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