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临床试验/IRCT2012102411245N1
IRCT2012102411245N1已完成未知

To compare outcomes of oral feeding 2 and 8 hours after cesarean section under regional anesthesia in term pregnant women

Kermanshah University of Medical Sciences (KUMS )0 个研究点目标入组 140 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
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
17 years 至 41 years(—)
性别
Female

入选标准

  • Pregnant women more than 37 weeks; elective cesarean section; regional anesthesia; after signing the informed consent.
  • Exclusion criteria:
  • Emergency cesarean section; general anesthesia; more than 1000 ml blood loss during operation; use of magnesium sulfate; gastrointestinal disorders and complications during surgery such as bowel and bladder injury.

排除标准

  • 未提供

研究者

发起方
Kermanshah University of Medical Sciences (KUMS )

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