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临床试验/PACTR202301645957324
PACTR202301645957324招募中未知

A randomised controlled trial comparing Erector Spinae and Transversus Abdominis Plane blocks for postoperative analgesia after elective caesarean section

未提供0 个研究点目标入组 66 人开始时间: 2023年1月9日最近更新:

试验速览

阶段
未知
状态
招募中
入组人数
66

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
19 Year(s) 至 44 Year(s)(—)
性别
Female

入选标准

  • Elective caesarean section.
  • Adult patients = 18 years of age.
  • ASA I - III.

排除标准

  • Emergency Caesarean Section.
  • BMI =35 (Taken at time of consent).
  • Patients that do not give signed informed consent to participate.
  • Contra-indication to spinal anaesthesia.
  • Contra-indication to local anaesthetic agent or opioids.
  • Patients requiring conversion from spinal anaesthesia to general anaesthesia at any stage during the caesarean section.
  • Patients with any physical or mental impairment which prevents them from being able to use a patient-controlled analgesia (PCA) pump postoperatively.
  • Patients with pre-existing chronic pain syndromes.

研究者

发起方
未提供

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