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临床试验/JPRN-UMIN000009939
JPRN-UMIN000009939已完成未知

Investigation of the optimum rate of patient controlled epidural analgesia after cesarean section - Investigation of the optimum rate of patient controlled epidural analgesia after cesarean section

Asahikawa Medical University0 个研究点目标入组 27 人开始时间: 2013年4月1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
27

研究概览

简要总结

The study has been terminated due to lack of participant.

研究设计

研究类型
Interventional

入排标准

年龄范围
20years-old 至 50years-old(—)
性别
Female

入选标准

  • 未提供

排除标准

  • Ptient refusal; known fetal anomalies; contraindication for combined spinal-epidural anesthesia because of hemodynamic, infectious, hemostatic, or neurological problems; severe preeclampsia; contraindication for the drugs used in the protocol; or failure of combined spinal-epidural anesthesia

研究者

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