Actively Recruiting
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
Eligibility Criteria
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
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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
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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