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ENROLLING BY INVITATION
NCT06200571

Biological Changes Associated With High Risk of Preeclampsia in Nulliparous Women

Sponsor: Norwegian University of Science and Technology

View on ClinicalTrials.gov

Summary

Primary outcome 1. to identify biological changes in nulliparous women at high risk for preeclampsia defined by combined screening by Fetal Medicine Foundation (FMF) 2. to identify biological effects of aspirin in nulliparous women with high risk for preeclampsia Secondary outcomes include findings of longitudinal development and predictive potential of biological markers associated with high-risk for preeclampsia and aspirin treatment. The main questions it aims to answer are: * Is high risk for preeclampsia associated with biological changes during pregnancy? * How does aspirin modulate the biological changes associated with high risk for preeclampsia? Nulliparous women will undergo routine clinical care at two regional hospitals with different treatment strategies, and selected to the study in three groups: low risk of preeclampsia, high risk of preeclampsia without aspirin, and high-risk of preeclampsia with aspirin treatment.

Official title: Characterization of the Immunological and Vascular Effects of Aspirin in Prevention of Preeclampsia in High-risk Nulliparous Women

Key Details

Gender

FEMALE

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

200

Start Date

2024-05-22

Completion Date

2032-12-31

Last Updated

2025-12-12

Healthy Volunteers

Yes

Conditions

Locations (2)

Alesund Hospital

Ålesund, Norway

St. Olavs Hospital

Trondheim, Norway