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临床试验/CTRI/2021/07/034930
CTRI/2021/07/034930尚未招募4 期

Randomized control trial comparing analgesia using continuous adductor canal block versus continuous epidural infusion in patients with unilateral total knee arthroplasty.

il0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1.American Society of Anaesthesiologists (ASA) grade 1, 2, 3 of unilateral total knee
  • arthroplasty.
  • 2.Age group of 30 â?? 90 years of both sexes.
  • 3.Patients giving valid informed consent.

排除标准

  • 1.Patient refusal.
  • 2.Bilateral total knee arthroplasty.
  • 3.Both epidural and adductor canal catheter used.
  • 4.Body mass index (BMI) greater than 40.
  • 5.History of drug or alcohol abuse and drug allergy, physically dependent on narcotics.
  • 6.Contraindication to either spinal or general anaesthesia.
  • 7.Patients with localized skin sepsis, haemorrhagic diathesis or neurological
  • involvement/ diseases.
  • 8.Patients with significant spinal deformity, history of chronic backache and headache.

研究者

发起方
il

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