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临床试验/DRKS00019069
DRKS00019069已完成4 期

IPACK (interspace between the popliteal artery and the capsule of the posterior knee) block efficiency as aid for ACB (Adductor Canal block) in postoperative analgesia after total knee arthroplasty (pilot study)

Hospital of Traumatology and Orthopaedics / University of Latvia0 个研究点目标入组 18 人开始时间: 2019年11月11日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
18

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomized controlled study
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 75 Years(—)
性别
All

入选标准

  • 1)Planned, unilateral, total knee arthroplasty
  • 2)Age 18-75 years
  • 3)BMI <35 kg/M2
  • 4)ASA score < IV
  • 5)Preoperative level of Hemoglobin >120 g/L
  • 6)Patient is motivated to follow the rules of study

排除标准

  • 1)Allergy to drugs used in study
  • 2)Myocardial infarction, pulmonary embolism, deep vein thrombosis, diabetes, atrial fibrillation, artificial cardiac pacemaker, neurological problems or problems of equilibrium
  • 3)Continuous use of anticoagulants before operation
  • 4)Steroid therapy during year before surgery
  • 5)Active malignancy
  • 6)Patient has been already included in a different study

研究者

发起方
Hospital of Traumatology and Orthopaedics / University of Latvia

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