跳至主要内容
临床试验/CTRI/2024/01/061363
CTRI/2024/01/061363已完成2/3 期

A comparative study between lateral transversus abdominis plane block versus a dual(lateral+ subcostal) transversus abdominis plane block for post operative analgesia in renal recipients- A prospective randomized controlled study

Priyanka Sarkar1 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2024年1月18日最近更新:

试验速览

阶段
2/3 期
状态
已完成
发起方
入组人数
75
试验地点
1
主要终点
Assess opioid requirement in post operative period up to 24 hours

研究概览

简要总结

This study is a prospective randomised controlled trial where we compare the effect of lateral and dual( lateral+ subcostal) transversus abdominis plane blocks on post operative analgesia in renal recipients.

The primary outcome is to assess opioid requirement in the first 24 hours of post operative period.

The secondary outcome is to assess the VAS scores, nausea and sedation scores in the first 24 hours of post operative period.

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
Participant and Investigator Blinded

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • Patients with American Society of Anaesthesiology physical status 3 posted for renal transplantation and consent taken for USG guided transversus abdominis plane block.

排除标准

  • Patient’s refusal to take part in our study Allergy to any drug administered in study History of seizures or fits History of CNS disease with potential for increase in intracranial pressure Chronic exposure to, or abuse of alcohol or other drugs affecting the CNS Use of any experimental drug within the last 30 days Patients with addiction to opioids Patients with long term usage of anti depressants, anti psychotics, anti convulsants Patients with coagulopathy and hepatomegaly Patients taken for re exploration after renal transplantation.

结局指标

主要结局

Assess opioid requirement in post operative period up to 24 hours

时间窗: 6 hours, 12 hours, 24 hours

次要结局

  • Assess visual analogue scale scores in the first 24 hours of post operative period(6 hours, 12 hours, 24 hours)
  • Assess nausea and sedation scores in the first 24 hours of post operative period(6 hours, 12 hours, 24 hours)

研究者

发起方
Priyanka Sarkar
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Priyanka Sarkar

Indraprastha Apollo Hospital, New Delhi

研究点 (1)

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