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临床试验/TCTR20220215009
TCTR20220215009Unknown4 期

Subcutaneous versus intravenous fentanyl for labor pain management A multicenter randomized controlled trial

Khon Kaen University0 个研究点目标入组 226 人开始时间: 2022年2月15日最近更新:
适应症

试验速览

阶段
4 期
入组人数
226

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

  • 1.pregnant women who 18 years old or older
  • 2. gestational age between 37 - 41 weeks 6 days
  • 2. plan vaginal delivery
  • 3. singleton pregnancy with cephalic presentation
  • 4. no obstetric or medical complication
  • 5. require medication for labor pain relief
  • 6. cervix open 4-9cm.

排除标准

  • 1. pregnant women who have fetal anomaly
  • 2. pregnant women who receive pethidine or morphine 24 hour prior
  • 3. pregnant women who addict opioid drugs
  • 4. pregnant women who receive any psychosis drugs 14 days prior admission
  • 5. pregnant women who have epilepsy and on enzyme CYP 3A4 inducers drugs such as carbamazepine, phenytoin ,rifampin
  • 6. pregnant women who have underlying disease such as liver disease heart disease respiratory tract infection
  • 7. pregnant women who do not understand Thai language

研究者

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