IRCT20180819040830N3已完成未知
Comparison of Efficacy and Safety of Cervical Pessary with Routine Management in Decreasing the Preterm Labor Rate in Nulliparous Symptomatic Pregnant Women with Short Cervix: A Randomized Clinical Trial
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 100
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 no limit（—）
- 性别
- Female
入选标准
- •Gestational age between 24 weeks and 0 days to 34 weeks and 0 days
- •Shortened cervical length (defined as cervical length =25 mm measured by trans-vaginal ultrasound scan in second trimester)
排除标准
- •Major fetal abnormalities
- •Fever or any other clinical findings in favor of chorioamnionitis and
- •Placenta previa
- •Women with normal cervical length
- •Women who had not responded to the routine standard treatments of preterm labor and were experiencing continued signs and symptoms of preterm labor after 48 hours of admission
- •Vaginal bleeding
- •Signs of ruptured membranes.
研究者
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