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临床试验/EUCTR2009-017441-63-IT
EUCTR2009-017441-63-IT进行中(未招募)不适用

EVALUATION OF PROGESTERONE-RELATED COMPOUNDS FOR THE TERZIARY PROPHILAXYS OF PRETERM DELIVERY: A MULTICENTRE RANDOMIZED CONTROLLED TRIAL - PROGESTERONE-RELATED COMPOUNDS AND PRETERM DELIVERY

.O. Ginecologia e Ostetricia0 个研究点开始时间: 2010年3月11日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)

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

  • Women with singleton pregnancy at 22nd to 32nd week of gestation presenting with a cervical length ≤25 mm, even after an episode of preterm labour.
  • 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 previous spontaneous PTD, multiple pregnancy, rupture of membranes, feto-maternal conditions indicating delivery, cervix dilated >2 cm or shorter than 5 mm, presence of regular uterine contractions.

研究者

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