跳至主要内容
临床试验/TCTR20210813001
TCTR20210813001Enrolling By Invitation4 期

The comparison of efficacy between intrathecal morphine combined with either selective COX-II inhibitor or acetaminophen and intrathecal morphine alone for analgesia after cesarean section: a randomized control trial

/A0 个研究点目标入组 88 人开始时间: 2021年8月13日最近更新:
适应症

试验速览

阶段
4 期
状态
Enrolling By Invitation
发起方
入组人数
88

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 40 Years(—)
性别
Female

入选标准

  • 1. Female participant age 18-40 years old undergoing elective cesarean section
  • 3. BMI 18-40 kg/m2

排除标准

  • 1. Patient deny
  • 2. Unable to communicate with researcher
  • 3. Medication allergy or contraindication to medication which will be administered in this study
  • 4. Contraindication of spinal anesthesia
  • 5. Chronic opioid user

研究者

发起方
/A

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