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临床试验/NCT07276646
NCT07276646招募中不适用

Perioperative Opioid-sparing Effect of Retrosuperior Costotransverse Ligament Block Versus Erector Spinae Block in Laparoscopic Cholecystectomy: A Randomized Clinical Trial.

Zagazig University1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2025年12月10日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
80
试验地点
1
主要终点
The time to first call to rescue analgesia

研究概览

简要总结

This study aims to compare the analgesic effect of retro superior costotransverse ligament space block vs erector spinae plane block to Achieve high-quality perioperative opioid-sparing effect and postoperative analgesia after laparoscopic cholecystectomy with optimum hemodynamic stability and high patient and surgeon satisfaction

详细描述

This study aims to compare between retro superior costotransverse ligament space block vs erector spinae plane block

  • To compare the analgesic outcomes (time to first analgesic request, total amount of analgesic consumption and pain scores by NRS)
  • To assess the block performance time required to perform each technique .
  • To compare intraoperative parameters (hemodynamics and intraoperative fentanyl consumption)
  • To assess patient, surgeon satisfaction and complications of the block.

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
Double (Participant, Outcomes Assessor)

盲法说明

anesthesiologist not sharing in the study will assess outcomes

入排标准

年龄范围
21 Years 至 64 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • patient acceptance
  • Age: 21-64 years old.
  • Sex: both sexes.
  • Physical status: ASA I & II.
  • Body mass index (BMI): 18.5 - 30 kg/m
  • Type of operations: elective laparoscopic cholecystectomy.
  • Duration of surgery not more than 2 hours.

排除标准

  • Known hypersensitivity to lidocaine or bupivacaine.
  • Patients with respiratory insufficiency.
  • Coagulation disorders or taking drugs affect surgical hemostasis.
  • 7. Patients with pre-existing neurological deficits.
  • Uncooperative patient or with altered mental status.
  • Patient with advanced cardiovascular or respiratory diseases

结局指标

主要结局

The time to first call to rescue analgesia

时间窗: 24 hours

The time to first call to rescue analgesia( the interval between the block injection till the NRS more than or equal 4) (naluphine) will be recorded

次要结局

  • To assess block characteristics (block performance time)(1 hour)
  • Total intraoperative fentanyl consumption(duration of surgery (up to 2 hours))
  • Pain intensity by Numerical Rating Scale(30 minutes after arrival to post anesthesia care unit , 2hours, 4hours, 6hours, 8hours, 12hours, 18 hours and 24hours postoperative)
  • total amount of rescue analgesia(24 hours)
  • Intraoperative hemodynamics (Heart Rate and Mean Arterial Pressure)(every 5 minutes in the first 30 minutes then every 10 minutes till the end of surgery)
  • Patient's satisfaction(24 hours)
  • complication of the block(24 hours)

研究者

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

Dina Abdelhameed Elsadek Salem

Associate professor

Zagazig University

研究点 (1)

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