Trial Parameters
Condition Pregnancy Complications
Sponsor University Hospital, Ghent
Study Type INTERVENTIONAL
Phase N/A
Enrollment 250
Sex FEMALE
Min Age 18 Years
Max Age N/A
Start Date 2019-04-01
Completion 2024-12-31
Interventions
Blood samples
Brief Summary
The aim of this study is the early (presymptomatic) detection of pregnancy complications, which could contribute to a preventive treatment.
Eligibility Criteria
Inclusion Criteria: * Every pregnant woman, speaking and understanding Dutch, French or English Exclusion Criteria: * not able to understand and adhere to the informed consent and study procedures