跳至主要内容
临床试验/CTRI/2022/11/047157
CTRI/2022/11/047157已完成3 期

To study the efficacy of 6% hydroxyethyl starch(HES) with 0.25% ropivacaine for ilioinguinal/iliohypogastric block along with wound infiltration in prolonging duration of post operative analgesia in paediatric unilateral inguinal hernia repair

All India Institute of Medical Sciences0 个研究点目标入组 50 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
已完成
入组人数
50

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)Age 1 to 7 years.
  • 2)Undergoing inguinal hernia surgeries.
  • 3)ASA I and ASA II category patients.
  • 4)All those parents or legal guardians giving consent.

排除标准

  • 1)Parent or guardian refusal.
  • 2)Patients with history of coagulation disorder.
  • 3)Infection at proposed IL/IH block.
  • 4)Pre-existing neurological disease.
  • 5)Known allergy to the local anesthetic or hydroxyethyl starch.

研究者

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