跳至主要内容
临床试验/EUCTR2006-000503-41-AT
EUCTR2006-000503-41-AT进行中(未招募)不适用

The PREDICT Study: The PREterm Delivery In Twins StudyEffectiveness of vaginally administered progesterone to prevent preterm delivery in twin pregnancies – A multicentre randomized trial - PREDICT

Rigshospitalet, Ultrasound Clinic 40230 个研究点目标入组 750 人开始时间: 2006年5月15日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
750

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

  • 1) Twin pregnancy
  • 2) Informed consent
  • 3) 18-23 weeks’ gestation
  • 4) Participants must be able to speak and understand the language spoken in the respective centres
  • 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

  • 1) Age < 18 years
  • 2) Known allergy to progesterone or peanuts
  • 3) Active thromboembolic disorders or a history of hormone-associated thromboembolic disorders
  • 4) Rupture of membranes at the time of inclusion
  • 5) Monoamniotic twins
  • 6) Pregnancies treated for or with signs of twin-to-twin transfusion syndrome at inclusion
  • 7) Multiple pregnancies reduced to twin pregnancies
  • 8) Known significant structural or chromosomal fetal abnormality
  • 9) Chorionicity not assessed before 15 weeks
  • 10) Known or suspected malignancy in genitals or breasts
  • 11) Known liver disease

研究者

发起方
Rigshospitalet, Ultrasound Clinic 4023

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