跳至主要内容
临床试验/TCTR20200228003
TCTR20200228003尚未招募未知

A Randomized Comparison Between Erector Spinae Plane Block and Intrathecal Morphine for Analgesia after Cesarean Delivery

Thammasat University Hospital0 个研究点目标入组 140 人开始时间: 2020年2月28日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
入组人数
140

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
18 Years 至 45 Years(—)
性别
Female

入选标准

  • â–ªOnly women able to provide informed consent will be recruited for study participation
  • â–ªPatients between 18 and 45 years
  • â–ªPatients undergoing elective lower segment (transverse incision) cesarean sections under spinal anesthesia

排除标准

  • â–ªASA patients greater than or equal to 3.
  • â–ªAllergies to local anesthetics
  • â–ªContraindication of neuraxial analgesia.
  • â–ªPatients with hemodynamic instability
  • â–ªPatients with systemic diseases: Coagulopathies, chronic use of analgesics, hypertensive disorders.
  • â–ªPatients with chronic pain
  • â–ªPatients with inability to comprehend or use the Numeric Rating Scale pain scoring system and difficulty to evaluate pain
  • â–ªPatients unable to communicate in English or French (in Thai for Thammasat University center)
  • â–ªIllness associated with pregnancy or high obstetric risk (gestational diabetes, pre-eclampsia, oligo and polyhydramnios, multiple pregnancy, anatomic malformations, etc.)

研究者

相似试验