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临床试验/NCT06987110
NCT06987110已完成不适用

A Randomized Clinical Trial Comparing Transverse Thoracic Plane Block, Midpoint Transverse Process Plane to Pleura Block and Erector Spinae Plane Block for Analgesia in Patients Undergoing Thoracoscopic Sympathectomy

Tanta University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年5月24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
60
试验地点
1
主要终点
Time to the 1st rescue analgesia

研究概览

简要总结

This study compares the transversus thoracic muscle plane block (TTPB), midtransverse to pleura block (MTPB), and erector spinae plane block (ESPB) for postoperative analgesia in patients undergoing thoracoscopic sympathectomy.

详细描述

Thoracoscopic sympathectomy is a well-established procedure for the treatment of various hyperhidrosis disorders and certain vascular conditions, involving the division of sympathetic nerve fibers in the thoracic cavity.

The erector spinae plane block (ESPB) is an interfascial regional anesthesia block for thoracic analgesia which can be performed by superficial or deep needle approach.

The mid-transverse to pleura block (MTPB) was first described as a modified paravertebral block.

Transversus thoracic muscle plane block (TTPB) is a newly developed technique in which LA is injected into the fascial plane between the transversus thoracic muscle and the internal intercostal muscles for blocking the anterior cutaneous branches of intercostal nerves from thoracic (Th) 2 to Th 6.

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

入选标准

  • •Age from 18 to 65 years.
  • •Both sexes.
  • •American Society of Anesthesiology (ASA) physical status I-II.
  • •Scheduled for thoracoscopic sympathectomy

排除标准

  • •Coagulopathy.
  • •History of opiate abuse.
  • •Pre-existing chronic pain.
  • •Allergy to local anesthetics or analgesics.
  • •Infection at the site of injection.
  • •Mental or neurological disorders.
  • •Pregnancy

研究组 & 干预措施

Transverse thoracic plane block group

Experimental

Patients will receive a transverse thoracic plane block.

干预措施: Transverse thoracic plane block (Other)

Midpoint transverse process plane to pleura block group

Experimental

Patients will receive a midpoint transverse process plane to pleura block.

干预措施: Midpoint transverse process plane to pleura block (Other)

Erector spinae plane block group

Experimental

Patients will receive an erector spinae plane block.

干预措施: Erector spinae plane block (Other)

结局指标

主要结局

Time to the 1st rescue analgesia

时间窗: 24 hours postoperatively

Time to the first request for the rescue analgesia (time from end of surgery to first dose of morphine administrated)

次要结局

  • Degree of patient satisfaction(24 hours postoperatively)
  • Total morphine consumption(24 hours postoperatively)
  • Degree of pain(24 hours postoperatively)
  • Heart rate(Till the end of surgery (Up to 2 hours))
  • Mean arterial pressure(Till the end of surgery (Up to 2 hours))
  • 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

Mahmoud Abdalsattar Elmohasseb

Lecturer of Anesthesiology, Surgical Intensive Care and Pain Medicine, Faculty of Medicine, Tanta University, Tanta, Egypt.

Tanta University

研究点 (1)

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