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临床试验/NCT05272280
NCT05272280招募中不适用

Ultrasound Guided External Oblique Intercostal (EOI) Block Versus Erector Spinae Plane Block (ESPB) for Postoperative Analgesia in Laparoscopic Cholecystectomy

Assiut University2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2022年5月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
50
试验地点
2
主要终点
Nalbuphine consumption in mg equivalent to morphine dose.

研究概览

简要总结

To compare the efficacy of USG-guided bilateral External oblique intercostal (EOI) block with Erector spinae plane block (ESPB) for post-operative analgesia after laparoscopic cholecystectomy with a hypothesis that both External oblique intercostal fascial plane block and Erector spinae plane block are effective in providing post-operative analgesia.

研究设计

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

盲法说明

triple

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age between 18 and 65 years with a body mass index (BMI) of 18-35 kg/m2,
  • patients with the American Society of Anesthesiologists (ASA) physical status I/II,
  • Patients scheduled for elective laparoscopic cholecystectomy.

排除标准

  • Allergy to local anaesthetics,
  • Infection at the site of injection,
  • Coagulopathy,
  • Chronic pain syndromes,
  • Prolonged opioid medication,
  • Patients who received any analgesic 24 h before surgery.

结局指标

主要结局

Nalbuphine consumption in mg equivalent to morphine dose.

时间窗: 24 hours postoperatively

mg

次要结局

  • Heart Rate(Intraoperatively at 0, 5,10, 20, and 30 minutes. Then every 15 min thereafter till the end of surgery)
  • Mean Arterial Pressure(Intraoperatively at 0, 5,10, 20, and 30 minutes. Then every 15 min thereafter till the end of surgery)
  • Shoulder pain(24 hours postoperatively)
  • Numerical Rating Scale (NRS) at rest and when coughing(at 1, 2,4 , 8, 16 and 24 hours postoperatively)
  • Incidence of Postoperative nausea & vomiting (PONV)(24 hours postoperatively)
  • Analgesic drug consumption other than nalbuphine(24 hours postoperatively)

研究者

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

Magdy Mohammed Mahdy Sayed

Doctor

Assiut University

研究点 (2)

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