LimPrOn: Limburg Pre-eclampsia Investigation

Recruiting N/A Interventional Study
Pregnancy Pre-eclampsia
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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At a Glance
Age
18 – 50
Sex
Female
Study type
Interventional
Purpose
Prevention
Participants needed
2,000 (estimated)
Sponsor
Hasselt University · Other
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About This Trial
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 g…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * \> 10 weeks of pregnancy, primipara and multipara Exclusion Criteria: * \< 10 weeks of pregnancy and congenital malformations of the fetus
Contacts

Dorien Lanssens, drs.

dorien.lanssens@uhasselt.be

CONTACT