Prospective Study in Pregnant Women With Hypercoagulopathy

Status Recruiting

Clinical Trial Summary

Pre-eclampsia is one of the most common causes of maternal and fetal morbidity and mortality. The aim of this study is to identify pregnant women at risk for pre-eclampsia or other cardiovascular complications at a very early state of the disease, and thereby improve the current method of screening.

Clinical Trial Description

600 pregnant women will be included in the project and followed in a standardized manner during their pregnancy. On a regular basis blood- and urine samples will be taken throughout their pregnancy and until 1 month after delivery and analyzed for a large variety of coagulation factors in order to identify factors that might predict an increased risk of developing pre-eclampsia and/or cardiovascular events. In addition a DNA-sample is taken if consented in order to evaluate genetic factors. ;

Study Design

Observational Model: Case Control, Primary Purpose: Screening, Time Perspective: Longitudinal

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00215969
Study type	Observational
Source	Hillerod Hospital, Denmark
Contact	Anita S Andersen, MD
Phone	+45 4829 6828
Email	asan@fa.dk
Status	Recruiting
Phase	N/A
Start date	January 2004
Completion date	October 2007

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