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临床试验/EUCTR2020-005126-28-BE
EUCTR2020-005126-28-BE进行中(未招募)1 期

Comparison of ultrasound-guided PENG block and supra-inguinal fascia iliaca compartment block for postoperative pain and early motor recovery after total hip arthroplasty: a randomized controlled non-inferiority clinical trial - Non-inferiority trial for PENG vs SFICB on pain and early motor recovery after THA

CHU de Liège0 个研究点目标入组 100 人开始时间: 2021年6月16日最近更新:
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
100

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Patients >18 years old
  • Classified as ASA 1-2-3
  • Admitted for elective total hip arthroplasty surgery by poster-lateral approach under spinal anesthesia
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 50
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 50

排除标准

  • Exclusion criteria included refusal of the patient and contraindications to the performance of SFICB or PENG block such as known allergy to used medications or local infection.
  • Other exclusion criteria included pregnancy, obesity with body mass index > 35, emergency hip arthroplasty or previous surgery on the same joint,
  • history of drug addiction, treatment with corticosteroids for more than 6 months, uncontrolled systemic arterial hypertension, severe kidney or liver diseases, and mental disorders or serious neurological diseases.

研究者

发起方
CHU de Liège

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