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临床试验/IRCT2016010325821N1
IRCT2016010325821N1已完成2 期

Comparing effect of the neuraxial painless vaginal delivery with vaginal delivery on fetal outcomes with due attention to newborns' APGAR scores in first, fifth and tenth minutes

Vice Chancellor for Research of Tabriz University of Medical Sciences0 个研究点目标入组 300 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
300

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
15 years 至 45 years(—)
性别
Female

入选标准

  • There is a possibility of natural birth; There is labor pain and active delivery phase; mother's consent to reduce delivery pain; spouse consent.
  • Exclusion criteria: mother's disinclination to participate; Inability to maintain immobility during procedure; Coagulation disorders and defects in homeostasis; Increased intracranial pressure for any reason; Frank infection at the needle site; Hypersensitivity to local anesthetics or other medications using in this methods; Acute lesions of the central nervous system; Maternal hemodynamic instability (hypovolemia, hypotension); Heart diseases that cardiac output is severely limited; fetal distress.

排除标准

  • 未提供

研究者

发起方
Vice Chancellor for Research of Tabriz University of Medical Sciences

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