跳至主要内容
临床试验/EUCTR2008-002792-28-NL
EUCTR2008-002792-28-NL进行中(未招募)不适用

Differences in maternal temperature and saturation after administration of remifentanil PCA or epidural analgesia during labor - differences in maternal temperature and saturation after administration of remifentanil PCA or epidu

eiden University Medical Center0 个研究点开始时间: 2008年6月4日最近更新:
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
Female

入选标准

  • Age =18 years
  • Between 37-42 weeks of gestation
  • Singleton pregnancy
  • ASA physical status I or II
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Prior administration of regional of opioid analgesia (during this delivery).
  • Morbid obesity (BMI = 40 kg/m2)
  • Drug allergy: history of hypersensitivity to opioid or local anesthetic substances
  • High risk pregnancy: including severe asthma (daily use of medication), insulin dependent diabetes, severe pre-eclampsia (proteinuria = 5 grams)
  • Use of antibiotics during delivery
  • Initial maternal SpO2 of less than 98%
  • Initial maternal temperature of 38°C or higher.
  • Cervical dilation of > 7 cm
  • Ruptured membranes for more than 24 hours at time of inclusion
  • Contraindication for epidural analgesia

研究者

发起方
eiden University Medical Center

相似试验