LimPrOn: Limburg Pre-eclampsia Investigation

  • STATUS
    Recruiting
  • End date
    Dec 24, 2030
  • participants needed
    2000
  • sponsor
    Hasselt University
Updated on 24 January 2021
hypertension
prenatal
proteinuria
eclampsia
toxemia of pregnancy

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

Details
Condition Pre-Eclampsia, Pregnancy, Preeclampsia, toxemia of pregnancy
Treatment Remote Monitoring
Clinical Study IdentifierNCT03509272
SponsorHasselt University
Last Modified on24 January 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Is your age between 18 yrs and 50 yrs?
Are you female?
Do you have any of these conditions: Pre-Eclampsia or Preeclampsia or Pregnancy?
Do you have any of these conditions: Pre-Eclampsia or Pregnancy or Preeclampsia or toxemia of pregnancy?
> 10 weeks of pregnancy, primipara and multipara

Exclusion Criteria

< 10 weeks of pregnancy and congenital malformations of the fetus
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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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