Actively Recruiting
Antiphospholipid Syndrome and Postpartum Pulmonary Artery Pressure
Led by Insel Gruppe AG, University Hospital Bern · Updated on 2024-05-09
900
Participants Needed
1
Research Sites
314 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The primary goal of this observational study is to learn about postpartum pulmonary artery pressure in women who suffered from Preeclampsia and Antiphospholipid Syndrome. The main question it aims to answer is whether the conjunction of preeclampsia with obstetric antiphospholipid syndrome significantly foster the development of long-lasting pulmonary hypertension. Only participants who suffered from preeclampsia during pregnancy will be followed for a period up to 3 years postpartum. Researchers will compare women with or without obstetric antiphospholipid syndrome.
CONDITIONS
Official Title
Antiphospholipid Syndrome and Postpartum Pulmonary Artery Pressure
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age over 16 years
- Consent or waiver of consent according to study guidelines
- Diagnosis of preeclampsia, defined by new onset hypertension (blood pressure >140/90 mmHg after 20 weeks gestation) plus one or more of: proteinuria, low platelet count, elevated serum creatinine, twice normal liver enzymes, pulmonary edema, persistent headache, or visual symptoms
- Postnatal follow-up at the obstetrical and cardiology clinic, Inselspital Bern, Switzerland
You will not qualify if you...
- Age under 16 years
- Incomplete or ambiguous data that prevent confirmation of eligibility or analysis of primary endpoint
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Inselspital
Bern, Switzerland, 3010
Actively Recruiting
Research Team
E
Emrush Rexhaj, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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