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临床试验/EUCTR2012-002547-15-ES
EUCTR2012-002547-15-ES进行中(未招募)不适用

TILITY OF THE ocolytict MAINTENANCE TREATMENT IN THE MANAGEMENT OF THE THREAT OF PREMATURE

Instituto de Investigacion Sanitaria La Fe0 个研究点开始时间: 2012年9月14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)
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

  • Women with singleton pregnancies with intact membranes have passed an episode of APP (uterine contractions with cervical change) successfully treated with acute tocolysis with atosiban. Cervical length ? 25 mm
  • 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 50
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range
  • Women with singleton pregnancies with intact membranes have passed an episode of APP (uterine contractions with cervical change) successfully treated with acute tocolysis with atosiban. Cervical length ? 25 mm
  • 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 50
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Cervical dilation ? 3 cm, multiple gestation, maternal medical contraindication to tocolysis with nifedipine, atosiban or progesterone, or obstetric contraindication to tocolytic therapy (severe preeclampsia, intrauterine infection, placental abruption, fetal anomaly incompatible with life, fetal death).
  • Cervical dilation ? 3 cm, multiple gestation, maternal medical contraindication to tocolysis with nifedipine, atosiban or progesterone, or obstetric contraindication to tocolytic therapy (severe preeclampsia, intrauterine infection, placental abruption, fetal anomaly incompatible with life, fetal death).

研究者

发起方
Instituto de Investigacion Sanitaria La Fe

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