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临床试验/IRCT201512163027N29
IRCT201512163027N29已完成2 期

The effect of intramascular Hyoscine and Hyoscine-Promethazine on the duration of labour and deliveryoutcomes to nuliparous pregnant women(triple-blind randomize control trial)

Tabriz University of Medical Sciences0 个研究点目标入组 213 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
入组人数
213

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
18 years 至 35 years(—)
性别
Female

入选标准

  • 37-41 weeks for gestational age; begining uterus contraction spontaneus; 4-5 for dillatation; 50-60% for effasman; rupture aminiotic sac befor intervention but not more than 6h past from its rupture;
  • one twin; nulliparous(with/without abortion in previeus pregnancy); lack of problem and sick in this pregnancy(for example preeclampsia, diabet,...); lack of controandication for normal delivery(HSV, CPD, placenta previa,... ); lack of problem in fetuse(unormal presentation); normal BMI in this pregnancy; fetus weight in normal range(2500-4000) according sonography or clinical exam; lack of major hip tightness; cephalic presentation; major height at least 150cm; mather age(18-35)
  • lack of glocome in mather(according to mathers statement); outgoing criteria(sensitivity to Hyoscine, unwillingness to continiue investigation, unormalfetus presentation, epidural analgisia)

排除标准

  • 未提供

研究者

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