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临床试验/IRCT201602213027N35
IRCT201602213027N35已完成未知

Comparing parenteral 5% dextrose, ringer and oral intake on the duration of labor stages in nulliparous women: A double- blinded randomized, controlled trial

Tabriz University of Medical Sciences0 个研究点目标入组 201 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
入组人数
201

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

  • being nulliparous, ages 18-35, gestational age (38-41 weeks), singleton pregnancy with cephalic presentation, onset of first stage of labor and 3-4 cm dilated, spontaneous onset of labor, maternal first trimester body mass index 18.5 <BMI<24.9 kg/m2, normal maternal pelvis (according to the experts and the researchers examinations), clinical and ultrasound prediction of no fetal macrosomia (weight more than 4.5 kg). Exclusion criteria: women with labor induction (indications of induction of labor such as prolonged rupture of membranes (over 18 h), gestational hypertension, nonreassuring fetal status, diabetes or preeclampsia), high risk pregnancies (gestational diabetes, preeclampsia, heart or kidney diseases, IUGR, detachment or placenta praevia,. ..) evidence of chorioamnionitis (maternal fever over 38oc) and fetal distress (abnormal NST), intrauterine fetal death, use of epidural

排除标准

  • 未提供

研究者

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