Future risk of cardiovascular disease risk factors and events in women after a hypertensive disorder of pregnancy.
Laura Benschop, Johannes J Duvekot, Jeanine E Roeters van Lennep
https://pubmed.ncbi.nlm.nih.gov/31175138Actively Recruiting
Led by Insel Gruppe AG, University Hospital Bern · Updated on 2024-05-09
900
Participants Needed
1
Research Sites
N/A
Total Duration
Researchers are studying postpartum pulmonary artery pressure in women who experienced preeclampsia during pregnancy, focusing on those with and without obstetric antiphospholipid syndrome (oAPS). The study aims to understand if the combination of preeclampsia and oAPS increases the risk of long-lasting pulmonary hypertension. This observational study is conducted at a single center and follows women up to three years after delivery to explore cardiovascular outcomes and risks. Women in two groups—those with preeclampsia and oAPS, and those with preeclampsia without oAPS—are followed for three years postpartum. During this period, routine data including echocardiography images and 24-hour ambulatory blood pressure monitoring are collected. These diagnostic tests assess heart function and blood pressure to compare outcomes between the groups. Participants will undergo scheduled evaluations including clinical exams, echocardiography, blood pressure monitoring, and blood sampling. Researchers will analyze changes in systolic pulmonary artery pressure and systemic arterial blood pressure at three months and three years after delivery. The study also seeks to assess the prevalence of arterial hypertension and develop prediction models for cardiovascular risks in women who had preeclampsia. Data collection will continue through 2028, covering retrospective and prospective follow-up periods.
CONDITIONS
Antiphospholipid Syndrome and Postpartum Pulmonary Artery Pressure
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 3 years postpartum
Participants who had preeclampsia are observed, with routine data collected including echocardiography images and 24-hour ambulatory blood pressure monitoring to assess cardiovascular function.
Assessments between 3 months and 3 years after delivery
Total: 1 location
1
Inselspital
Bern, Switzerland, 3010
Actively Recruiting
E
Emrush Rexhaj, MD
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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