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临床试验/TCTR20150503001
TCTR20150503001已完成4 期

Cesarean Section Rate in Oxytocin Infusion between Continuous Until Delivery and Discontinuation at Active Phase of Labor: a Randomized Controlled Study

Bhumibol Adulyadej Hospital0 个研究点目标入组 340 人开始时间: 2015年5月3日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
入组人数
340

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
0 N/A (No limit) 至 0 N/A (No limit)(—)
性别
Female

入选标准

  • gestational age of 37 to 42 weeks, singleton with cephalic presentation, latent phase of labor, estimated fetal weight < 4000 g by Leopold�s maneuver or ultrasonography and bishop score > 4

排除标准

  • fetal malpresentation, previous cesarean section or uterine scar such as previous myomectomy, placenta previa, placental abruption, persistent non-reassuring fetal heart rate pattern, active phase of labor, premature rupture of membrane (PROM), documented fetal anomalies, severe maternal diseases or maternal complications such as severe pre-eclampsia, diabetes mellitus, heart disease, HIV infection, genital lesions that obstruct passage of labor such as large genital wart or active genital herpes and contracted pelvis.

研究者

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