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临床试验/NCT07351253
NCT07351253招募中不适用

Analgeisc Effect of Erector Spinae Plane Block Versus Lateral Transversus Abdominis Plane Block in Patients Undergoing Open Abendectomy Surgery: a Randomized Controlled Trial

Cairo University1 个研究点 分布在 1 个国家目标入组 68 人开始时间: 2026年1月25日最近更新:
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
68
试验地点
1
主要终点
Total morphine consumption

研究概览

简要总结

this aim of this study is to compare the analgesic effect of Erector spinae plane (ESP) block and lateral transversus abdominis plan (TAP) block in patients undergoing open appendectomy.

详细描述

regional technique according to randomization will be given after induction of general anesthesia Fentanyl boluses of 1 mcg/kg will be given in case of inadequate analgesia. Inadequate analgesia identified by 20% increase in the heart rate and/or systolic blood pressure from baseline measurement.

postoperative analgesia: regular paracetamol 1 g/6 hours (intravenously at first then orally once the oral feeding is resumed) and 75 mg diclofenac (intramuscularly at first then orally once the oral feeding is resumed).

If Numeric rating scale (NRS) is > 3 intravenous titration of 2 mg morphine is given slowly to be repeated after 30 minutes if pain persisted

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, Investigator, 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

入选标准

  • adult patients, undergoing open appendectomy.

排除标准

  • American society of anesthesiologist-physical status >III,
  • allergy to any of the study drugs,
  • coagulopathy
  • local infection,
  • history of chronic pain or regular opioid use;
  • inability to comprehend the Numeric Rating Scale (NRS),
  • pregnant or lactating women.

研究组 & 干预措施

ESP group

Active Comparator

干预措施: Erector Spinae Plane Block (Other)

TAP group

Active Comparator

干预措施: Transversus abdominis plane (TAP) block (Other)

结局指标

主要结局

Total morphine consumption

时间窗: from extubation until 24 hours postoperative

mg

次要结局

  • numeric rating scale(AT 0.5, 2, 6, 12, and 24 hours postoperative.)
  • quality of recovery(24 hours after suregry)

研究者

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

Ahmed Hasanin

Professor

Cairo University

研究点 (1)

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