Cardiovascular Risk Assessment in Young Women After Index Pregnancy With and Without Placental Complications

Recruiting Observational Study
Cardiovascular (CV) Risk Preeclampsia (PE) Fetal Weight
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Female
Study type
Observational
Participants needed
1,260 (estimated)
Sponsor
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau · Other
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About This Trial
In this project, the investigators aim to study how all these factors determine the cardiovascular status of a total of 1,800 mothers, 3 to 6 years after delivery. In addition, the investigators want to assess whether lifestyle and living conditions after childbirth may improve or worsen this imprint, since women often prioritize their families over themselves, making it more difficult to maintain…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Patients who participated in the BiSC (Barcelona Life Study Cohort), EuroPE (Randomized open-label control trial to evaluate if the incorporation of sFlt1/PlGF ratio in the diagnosis and classification of PE improves maternal and perinatal outcomes in women with suspicion of t…
Contacts

Elisa Llurba Olivé, PhD

+34 935534078

ellurba@santpau.cat

CONTACT

Pablo García Manau, PhD

+34 627813346

pgarciama@santpau.cat

CONTACT