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.
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