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临床试验/CTRI/2025/08/092850
CTRI/2025/08/092850尚未招募2/3 期

A Randomoised,Prospective, Double Blinded Study To Compare The Efficacy Of Ultrasound Guided Transversus Abdominis Plane Block and Erector Spinae Plane Block in Minimally Invasive Nephrectomy Surgeries

SRM Institutes For Medical Sciences1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2025年8月22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
50
试验地点
1
主要终点
1)To observe intraoperative Remifentanil requirement and the pain score using Visual Analog Scale (VAS) score for first 24 hours,postoperative Tramadol requirement for first 24 hours

研究概览

简要总结

This study is a randomised ,prospective,double blinded comparing the efficacy of ultrasound guided Transversus Abdominis Plane Block and Erector Spinae Plane Block in Minimally Invasive Nephrectomy Surgeries.Primary outcomes will be intraoperative Remifentanil requiremet,the pain score using Visual Analog Scale (VAS) score for first 24 hours,the postoperative Tramadol requirement for first 24 hours.secondary outcomes will be the incidence of hemodynamic disturbances during perioperative period,the incidence of side effects of opioids such as postoperative nausea, vomiting, sedation and respiratory depression.

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
20.00 Year(s) 至 70.00 Year(s)(—)
性别
All

入选标准

  • ASA grade 1 and 2,Any gender ,Age 20 to 70 years ,BMI 18 to 30 ,Patients willing to participate in the study ,Patients admitted for minimally invasive nephrectomy surgery ,No history of allergy to Local anaesthetics.

排除标准

  • ASA grade 3, 4, 5,Pregnant and lactating mother,Age less than 20 years and more than 70 years,Obese individuals with BMI more than 30,Chronic history of Opioid abuse,History of allergy to Local anaesthetics,Patients not willing to participate in this study.

结局指标

主要结局

1)To observe intraoperative Remifentanil requirement and the pain score using Visual Analog Scale (VAS) score for first 24 hours,postoperative Tramadol requirement for first 24 hours

时间窗: 12 months

次要结局

  • 1) To observe the incidence of hemodynamic disturbances during perioperative period(2) To observe the incidence of side effects of opioids such as postoperative nausea, vomiting, sedation and respiratory depression)

研究者

发起方
SRM Institutes For Medical Sciences
申办方类型
Private hospital/clinic
责任方
Principal Investigator
主要研究者

shanmugapriya g

SRM INSTITUTES FOR MEDICAL SCIENCES

研究点 (1)

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