跳至主要内容
临床试验/ISRCTN14256563
ISRCTN14256563已完成未知

Evaluating the satisfaction in parturients receiving epidural analgesia after prenatal shared decision-making intervention

Chi Mei Medical Center0 个研究点目标入组 200 人开始时间: 2020年4月15日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
200

研究概览

简要总结

2020 Results article in https://pubmed.ncbi.nlm.nih.gov/32689958/ results (added 22/07/2020)

研究设计

研究类型
Interventional

入排标准

性别
Female

入选标准

  • •Parturients after natural spontaneous delivery who have used epidural analgesia during the natural birth process

排除标准

  • •1. Mental disorders or emotional disorders, regardless of whether they are receiving psychiatric medication
  • •2. Drug addiction or drug dependence (for example, those who have a history of drug use, or who have used morphine analgesics daily for more than 30 mg of oral morphine equivalent for more than six weeks)
  • •3. Cannot read Chinese
  • •4. In the intensive care unit after delivery

研究者

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