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临床试验/NCT01195441
NCT01195441已完成不适用

Prediction and Prevention of Preeclampsia by First Trimester Ultrasound

Norwegian University of Science and Technology1 个研究点 分布在 1 个国家目标入组 602 人开始时间: 2010年9月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
602
试验地点
1
主要终点
Development of preeclampsia

研究概览

简要总结

The purpose of this study is to determine whether the Fetal Medicine Foundation algorithm for individual risk calculation for preeclampsia (PE) and pregnancy induced hypertension (PIH) is suitable to identify women in high risk of developing these diseases in a Norwegian population.

详细描述

It has been shown that low dose acetylsalicylic acid (ASA) in pregnancy reduces adverse outcome of pregnancy in women that have high risk of developing preeclampsia (PE). It is a challenge for the clinician to identify the high risk women. Doppler blood flow measurements in uterine arteries in second trimester have been shown useful to predict the development of the disease but prophylactic treatment with ASA from this point in pregnancy has not been proven effective. Fetal Medical Foundation has developed an algorithm that calculates individual risks for PE/ PIH based on Doppler blood flow measurements and anamnestic information.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Nulliparous
  • Para 1+ with previous preeclampsia or gestational hypertension
  • last menstrual period (LMP) pregnancy length at inclusion < 13 weeks
  • Residence in Trondheim + 8 surrounding municipalities

排除标准

  • Pregnancy length > 13+6 weeks (CRL > 85 mm)
  • Missed abortion
  • Fetal anomaly

结局指标

主要结局

Development of preeclampsia

时间窗: september 2012

Onset time of preeclampsia

时间窗: September 2012

次要结局

  • Gestational age at delivery(September 2012)
  • Number of induction of deliveries due to preeclampsia(September 2010)
  • Maternal morbidity(September 2012)
  • Perinatal morbidity(September 2012)
  • Number of instrumental deliveries due to preeclampsia(September 2012)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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