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
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)
