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临床试验/CTRI/2025/11/097196
CTRI/2025/11/097196尚未招募2/3 期

Comparison Of Peritubal Infiltration and USG guided Erector spinae Plane block for Post operative Analgesia in Percutaneous Nephrolithotomy -A prospective randomised controlled study

Dr D Tulja Bhavani1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年11月25日最近更新:

试验速览

阶段
2/3 期
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
To compare the need for first rescue analgesia in both groups- in patients receiving 0.375% Ropivacaine vs patients receiving peri tubal infiltration.

研究概览

简要总结

The primary aim of this study is to assess the VAS scores in population receiving 20ml of 0.375% Ropivacaine in erector spinae block versus population receiving 20ml of 0.375% Ropivacaine through peritubal infiltration in PCNL surgeries for post operative analgesia, to measure and compare the total analgesic consumption in both the groups.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Investigator Blinded

入排标准

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

入选标准

  • ASA-1and ASA-2patients of either sex
  • Patients of age between 18-60years of age
  • Patients posted for elective percutaneous nephrolithotomy under general Anaesthesia.

排除标准

  • 1.Patient refusal 2.Patients with known hypersensitivity to known local Anesthetic drug 3.Patients with bleeding diathesis , uncontrolled diabetes mellitus and severe hepatorenal disease .
  • Patients with epilepsy and mentally unstable patients 5.Pregnant and lactating women
  • Patients on chronic analgesic therapy and anticoagulants.
  • Patients with cardio respiratory, neurological or psychiatric illness.
  • Renal stones which require more than one puncture , supra coastal puncture intraoperative excessive bleeding 9.Surgical time more than 3hours 10.BMI morethan 35Kg/m2.

结局指标

主要结局

To compare the need for first rescue analgesia in both groups- in patients receiving 0.375% Ropivacaine vs patients receiving peri tubal infiltration.

时间窗: at 0,2,4,6,8,10,12,16,18 | and 24hours in both groups.

次要结局

  • to compare the total analgesic consumption(at 0,2,4,6,8,10,12,16,18 till 24 hours)

研究者

发起方
Dr D Tulja Bhavani
申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Dr D Tulja Bhavani

Rajarajeswari medical college and Hospital

研究点 (1)

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