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临床试验/PACTR202002616299138
PACTR202002616299138尚未招募4 期

Comparison of Spinal Morphine and Transverse Abdominis Plane Block for Postoperative Pain Management in Patients Undergone Cesarean Section Under Spinal Anesthesia : Randomized control trial

Dilla University0 个研究点目标入组 120 人开始时间: 2019年12月24日最近更新:
适应症

试验速览

阶段
4 期
状态
尚未招募
入组人数
120

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

  • Parturient who will undergo elective caesarean delivery
  • Pfannenstiel incision under spinal anaesthesia

排除标准

  • Patient refusal
  • ASA 3 and above
  • Caesarean delivery requiring epidural analgesia
  • Preeclamptic
  • Mothers with chronic pain disorder
  • history of benzodiazepines taking
  • history of opioid taking
  • infection at needle insertion site
  • coagulopathy disorder
  • hypovolemic patient
  • Allergy to local anaesthetics and morphine
  • Failed spinal block or difficulty
  • patients unable to self -report acute pain
  • Cognitive impairment (Dementia, Alzheimer

研究者

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