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Clinical Trials/NCT00215969
NCT00215969
Unknown
Not Applicable

Prospective Study of Hypercoagulation in Pregnant Women

Hillerod Hospital, Denmark2 sites in 1 country600 target enrollmentJanuary 2004

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pre-Eclampsia
Sponsor
Hillerod Hospital, Denmark
Enrollment
600
Locations
2
Last Updated
20 years ago

Overview

Brief 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.

Detailed 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.

Registry
clinicaltrials.gov
Start Date
January 2004
End Date
October 2007
Last Updated
20 years ago
Study Type
Observational
Sex
Female

Investigators

Sponsor
Hillerod Hospital, Denmark

Eligibility Criteria

Inclusion Criteria

  • Pregnant women attending the midwife at Hilleroed Hospital, Frederiksborg County, Denmark.

Exclusion Criteria

  • Mental disease.
  • Problems understanding or reading Danish.

Outcomes

Primary Outcomes

Not specified

Study Sites (2)

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