EUCTR2008-005987-15-NL进行中（未招募）不适用
Preventing preterm birth: Costs and effects of screening of healthy women with a singleton pregnancy for a short cervical length. - The Triple P study
AMC Amsterdam0 个研究点开始时间: 2008年10月30日最近更新:
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- Female
入选标准
- •-- Capacitated women
- •-- = 18 years old
- •-- Singleton healthy pregnancy
- •-- Two times a cervical length = 25 mm: a cervical length = 25 mm at 16-20 weeks gestation, and a confirmation of this result with a repeat measurement of the cervical length at 20-22 weeks gestation
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Women with a pregnancy with major foetal abnormalities, painful regular uterine contractions, a history of ruptured membranes or a cervical cerclage will be excluded. In addition, women with a previous preterm birth are excluded as well.
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