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LimPrOn: Limburg Pre-eclampsia Investigation — LimPrOn  

Pregnancy Clinical Trial

Official title:
LimPrOn: Limburg Pre-eclampsia Investigation

Clinical Trial Summary

Background: Multiple adaptations at the cardiovascular system occurs during pregnancy. In the pregnancy condition pre-eclampsia (PE), this adaptations are abnormal. Five to eight percent of all pregnant women worldwide will develop PE. PE is a pregnancy condition which is characterized with a high blood pressure (>140/90 mm Hg) and the occurrence of proteinuria (>3g/dl/24h) after 20 weeks of gestation. When untreated, this condition can have severe complications for both mother and child. It's important to monitor women with a high risk for developing PE for an early detection and treatment of this condition. For this reason, a multicenter study is set up with the following applications: 1. NICCOMO and Maternal Venous Doppler Echography: impedance cardiograph and an echography of the heart and veins. 2. Maltron: bio-electronic impedance analyze 3. Remote monitoring of the high risk patients to become a more intensive follow-up Number of inclusions: 2000 pregnant women from the prenatal consultations of eight different hospitals:

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03509272
Study type Interventional
Source Hasselt University
Contact Dorien Lanssens, drs.
Email dorien.lanssens@uhasselt.be
Status Recruiting
Phase N/A
Start date May 2016
Completion date December 2030
View Details
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