跳至主要内容
临床试验/NCT07738900
NCT07738900已完成不适用

Efficacy of Bilateral Modified Thoracoabdominal Nerve Block as an Analgesic Technique in Comparison With Bilateral Thoracic Erector Spinae Plane Block in Abdominoplasty Operations

Mansoura University1 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2024年12月1日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
48
试验地点
1
主要终点
Total opioid consumption

研究概览

简要总结

This study aimed to compare the analgesic effect of bilateral ultrasound-guided modified thoracoabdominal nerve block with bilateral ultrasound-guided erector spinae plane block in abdominoplasty surgery.

详细描述

Abdominoplasty is an extra-peritoneal surgery devoid of visceroperitoneal component of pain, most of pain is initially related to the abdominal wall's facial plication in addition to pain generated from the abdominal wall incision.

Ultrasound guided erector spinae plane block (ESPB) is considered relative an effective block that can be used to provide postoperative analgesia in abdominoplasty (Tulgar et al., 2018). Erector spinae plane block (ESPB) is an interfascial plane block was used to relieve chest neuropathic pain.

The modified thoracoabdominal nerve block through the perichondral approach (M-TAPA) is a novel regional nerve block that can provide optimal analgesia for both the lateral and anterior abdominal wall. It can provide wide range of analgesic coverage of the trunk (i.e., T7-T12) by a single puncture per side and has been initially reported to provide a longacting analgesia.

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)

入排标准

年龄范围
21 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Age between 21 and 60 years.
  • Both sexes.
  • American Society of Anesthesiologists physical status grade I and grade II.
  • Elective abdominoplasty operation.

排除标准

  • Patient refusal.
  • Local skin infection and sepsis at site of the block.
  • Known allergy to local anesthetic drugs.
  • Coagulopathy.
  • Psychiatric diseases.
  • Central or peripheral neurological disease.

结局指标

主要结局

Total opioid consumption

时间窗: 24 hours postoperatively

Intravenous pethidine (0.5mg/kg) was taken every 12 hours as rescue analgesia.

次要结局

  • Duration of analgesia(24 hours postoperatively)
  • Degree of pain(24 hours postoperatively)
  • Cortisol level(24 hours postoperatively)
  • C-reactive protein (CRP) level(24 hours postoperatively)
  • Incidence of complications(24 hours postoperatively)

研究者

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

Fatma Othman Ibrahim Yossef

Assistant Lecturer of Anesthesia and Surgical Intensive Care, Mansoura University, Egypt.

Mansoura University

研究点 (1)

Loading locations...

相似试验