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Prediction and Prevention of Preeclampsia by First Trimester Ultrasound — Screen-tox  

Preeclampsia Clinical Trial

Official title:
Prediction and Prevention of Preeclampsia by First Trimester Ultrasound

Clinical Trial Summary

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.

Clinical Trial Description

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. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01195441
Study type Observational
Source Norwegian University of Science and Technology
Contact
Status Completed
Phase N/A
Start date September 2010
Completion date October 2013
View Details
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