Origins, features, and effects of preeclampsia on mother and baby

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a prospective, single-center observational cohort enrolling about 50 pregnant women with clinically diagnosed preeclampsia per year at the Department of Obstetrics and Gynecology, Medical University of Graz. Participants attend up to four time points (diagnosis, late pregnancy, delivery sampling, and an 8–12 week postpartum visit) for clinical data collection, physical measurements, and biological sample banking. The protocol excludes pregnancies with major fetal anomalies and focuses on standardized phenotyping to link maternal clinical features, placental and blood biomarkers, and early neonatal outcomes. Collected data and samples aim to support detailed analyses of disease mechanisms and early-life consequences for mother and child.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Ongoing pregnancy with preeclampsia regardless the gestational age diagnosed for PE

Exclusion Criteria:

* Maternal or fetal genetic abnormalities

Where it's running

• Department of Obstetrics and Gynecology, Medical University of Graz
  Graz, Austria Recruiting

Study contacts

• Study coordinator: Christina Stern, Dr.med
• Email: christina.stern@medunigraz.at
• Phone: +43 316 385 86306

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.