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临床试验/CTRI/2023/02/050011
CTRI/2023/02/050011尚未招募不适用

Comparison of ultrasound guided External Oblique Intercostal Plane Block and Subcostal Transversus Abdominis Plane Block in patients undergoing upper abdominal surgery: A randomized clinical study

All India Institute of Medical Sciences, Patna1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2023年1月3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
50
试验地点
1
主要终点
Time to first rescue analgesic administration

研究概览

简要总结

This is a clinical trial to compare the analgesic efficacy of ultrasound guided External Oblique Intercostal Plane Block better and Subcostal Transversus Abdominis Plane Block in patients undergoing upper abdominal surgery. Group E will receive US-guided External Oblique Intercostal Plane block using 25ml of 0.2% Ropivacaine along with GA and Group T will receive US-guided Subcostal TAP block using 25ml of 0.2% Ropivacaine along with GA. Total  intraoperative fentanyl consumption will benoted in both groups. Time of block performance(TBP) will be observed in each group. Pain perception will be measured in the PACU atrest by using NRS (0–10) at 0,1,2,4,6,12, and 24 hour, total opioid consumption will be recorded and complications if any will be noted

研究设计

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

  • ASA I –II patients scheduled to undergo elective supra-umbilical surgeries with unilateral incision under GA.

排除标准

  • 1.BMI< 20 2.Allergy to local anesthetics 3.Infection at the site of injection 4.Chronic pain syndromes
  • Patients on chronic analgesic therapy 6.Chronic liver disease, chronic renal disease, and cognitive impairment.

结局指标

主要结局

Time to first rescue analgesic administration

时间窗: Time to first rescue analgesic administration

次要结局

  • Time of block performance (TBP)(Intraoperative fentanyl consumption)

研究者

发起方
All India Institute of Medical Sciences, Patna
申办方类型
Government medical college

研究点 (1)

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