跳至主要内容
临床试验/CTRI/2021/09/036352
CTRI/2021/09/036352尚未招募不适用

Comparative efficacy of postoperative pain relief between ultrasound guided Transversus abdominis plane block and Ilioinguinal & Iliohypogastric nerve blocks for patients undergoing open inguinal hernia repair under Spinal Anaesthesia.

VADDADI RAVITEJ1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2021年9月23日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
comparision of duration of post operative analgesia

研究概览

简要总结

This study is a Randomized, double blind, parallel group trail comparing the efficacy of postoperative pain relief between ultrasound guided transversus abdominis plane block and ilioinguinal plane & iliohypogastric nerve block in patients undergoing open inguinal hernia repair under spinal anaesthesia. This trial will be conducted in 60 patients with ASA grades I & II in India. The primary outcome is to measure and compare the duration of postoperative analgesia. Secondarily, to compare the quality of pain relief and requirement of rescue analgesia for the first 48 hours post operatively.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant and Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
Male

入选标准

  • 18 TO 60 Years. ASA Physical status grade.
  • I and II. Patients undergoing elective primary unilateral open inguinal hernia repair.

排除标准

  • Patient who refused to consent to study.
  • BMI > 40 kg/m2 Poorly regulated systemic diseases.
  • Local infection at the site of block.
  • Patients with hypersensitivity to local anaesthetic drugs.
  • Patients who will be scheduled for bilateral or recurrent inguinal hernia repair.

结局指标

主要结局

comparision of duration of post operative analgesia

时间窗: 48hrs post operatively

次要结局

  • compare quality of pain relief(upto 48hrs postoperatively)
  • requirement of rescue analgesia(upto 48hrs postoperatively)
  • incidence of any side effects(upto 48hrs postoperatively)

研究者

发起方
VADDADI RAVITEJ
申办方类型
Other [self]

研究点 (1)

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