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临床试验/NCT06710444
NCT06710444已完成不适用

Ultrasound-guided Erector Spinae Plane Block Versus Retrolaminar Block for Postoperative Analgesia in Patients Undergoing Percutaneous Nephrolithotomy

Alexandria University1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2024年12月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
120
试验地点
1
主要终点
measurement of visual analogue score

研究概览

简要总结

The study will investigate the effects of ultrasound-guided ESPB and RLB on intraoperative and postoperative analgesia in patients undergoing PCNL to identify a safe and effective regional block method for postoperative analgesia

详细描述

All the patients will be blinded to the intervention received in this study. All patients will receive standard general anesthesia technique with endotracheal intubation and muscle paralysis. Postoperatively, all patients will receive analgesia in the form of non-steroidal anti-inflammatory drugs and paracetamol. In case the VAS scores exceeded 4 in any group, the patients will receive rescue analgesia with 25 mg IV meperidine. In both groups, the ESPB and RLB will be performed after induction of general anesthesia using portable ultrasound device.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Outcomes Assessor)

入排标准

年龄范围
21 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients scheduled for PCNL

排除标准

  • •daily consumption of analgesics
  • •allergy to local anesthetics
  • •liver dysfunction
  • •infection or previous surgery in the vertebral region.
  • •patient refusal
  • •pregnancy

研究组 & 干预措施

Group I

Active Comparator

This group will receive ultrasound-guided erector spinae plane block

干预措施: ultrasound-guided erector spinae plane block (Procedure)

Group II

Experimental

This group will receive ultrasound-guided Retrolaminar plane block

干预措施: ultrasound-guided retrolaminar plane block (Procedure)

结局指标

主要结局

measurement of visual analogue score

时间窗: after the surgery average 48 hours postoperative

measurement of visual analogue score during rest and movement. The Score range from 0-10. 0 means no pain and 10 indicates the worst pain ever

次要结局

  • postoperative additional analgesic requirement(after the surgery average 48 hours postoperative)
  • assessing the patient satisfaction by a the short assessment of patient satisfaction score (SAPS)(after the surgery average 48 hours postoperative)
  • Time to ambulate(after the surgery average 12 hours postoperative)
  • presence of postoperative nausea and vomiting(after the surgery average 48 hours postoperative)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Ahmed Shehab, MD

Lecturer in Anaesthesia and Surgical ICU department

Alexandria University

研究点 (1)

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