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临床试验/IRCT20180227038892N1
IRCT20180227038892N1招募中未知

Comparison effect of oral Dydrogesterone on the treatment of preterm labor with oral Nifedipine in pregnant women admitted with a diagnosis of risk of preterm labor

Iran University of Medical Sciences0 个研究点目标入组 60 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
招募中
入组人数
60

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 45 years(—)
性别
Female

入选标准

  • A total of 60 women aged 18-45 years with a singleton pregnancy of 26-34 weeks, admitted with a diagnosis of preterm labor, are included in the study.

排除标准

  • Exclusion criteria include any maternal or fetal conditions that require immediate delivery (including fetal distress; placenta abruption; chorioamnionitis; severe preeclampsia; Patients who have entered the active phase of labor ( cervical dilatation>=4cm); vaginal bleeding; Ruptured of membrane; Uterine distention for example due to multiple pregnancy and polyhydramnios; The presence of any systemic infection; Fever greater than 38 degrees Centigrade; Intrauterine growth restriction; Blood pressure above 140/90 mm Hg; Fetal anomalies; Contraindications to the use of tocolytics, history of any allergy to progesterone and a history of any thromboembolic disease.

研究者

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