Actively Recruiting

Age: 18Years +
FEMALE
ID07513558

Face to Face With Preeclampsia: Understanding Its Origin, Characteristics and Effects on Mother and Baby

Led by Medical University of Graz · Updated on 2026-04-13

250

Participants Needed

1

Research Sites

261 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Preeclampsia (PE) is a serious pregnancy complication marked by new high blood pressure and signs of organ problems in the mother, often linked to issues with the placenta and blood vessel function. It can lead to negative outcomes for both mother and baby and increases long-term risks for heart and metabolic diseases. This study aims to create a detailed group of pregnant women diagnosed with PE to better understand the condition and its effects on mothers and infants. The study is observational and will follow about 50 women diagnosed with PE each year from their diagnosis through late pregnancy, delivery, and 8-12 weeks postpartum. Participants may have up to four study visits including optional visits after PE diagnosis and late in pregnancy, a visit at delivery for sample collection, and a postpartum follow-up. Researchers will collect clinical data, physical measurements, questionnaires, and biological samples such as blood, urine, saliva, vaginal swabs, breast milk, placental tissue, and umbilical cord samples. Participants and their babies will have assessments including blood pressure and heart function tests, body measurements, fetal growth scans, and questionnaires on lifestyle. Samples and data will be stored for future research. The main outcome measures include detailed assessments of the mother's metabolic and heart health from diagnosis through postpartum, as well as infant body composition and heart function at birth and postpartum. Data will be compared with healthy pregnancies for broader understanding.

CONDITIONS

Brief Title

Preeclampsia: Origin, Characteristics and Effects on Mother and Baby

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Pregnant women with a clinical diagnosis of preeclampsia at any gestational age
  • Women aged 18 years or older
  • Female participants
Not Eligible

You will not qualify if you...

  • Maternal or fetal genetic abnormalities

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surveillance

Duration - From diagnosis of preeclampsia through childbirth

Participants are observed and clinical data and biological samples are collected at multiple points during pregnancy and delivery to understand preeclampsia.

Up to 3 visits including an optional visit after diagnosis, an optional late pregnancy visit, and delivery visit

Long-term Monitoring

Duration - 8 to 12 weeks postpartum

Participants and their infants are followed up postpartum to collect clinical and biological data to assess early-life outcomes after preeclampsia.

1 follow-up visit (in-person)

Trial Site Locations

Total: 1 location

1

Department of Obstetrics and Gynecology, Medical University of Graz

Graz, Austria, 8036

Actively Recruiting

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Research Team

C

Christina Stern, Dr.med

U

Ursula Hiden, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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