Actively Recruiting

Age: 16Years +
FEMALE
ID05679206

Association Between Preeclampsia, Antiphospholipid Syndrome and Postpartum Pulmonary Artery Pressure, Systemic Arterial Pressure and Cardiovascular Function

Led by Insel Gruppe AG, University Hospital Bern · Updated on 2024-05-09

900

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

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

Brief Title

Antiphospholipid Syndrome and Postpartum Pulmonary Artery Pressure

Who Can Participate

Age: 16Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Female, age greater than 16 years
  • Diagnosis of preeclampsia during pregnancy, defined by new hypertension after 20 weeks gestation plus one or more specific clinical signs
  • Consent to participate or waiver of consent according to study guidelines
  • Postnatal follow-up at the obstetrical and cardiology clinic, Inselspital Bern, Switzerland
Not Eligible

You will not qualify if you...

  • Age under 16 years
  • Incomplete or ambiguous data that prevents confirmation of eligibility or analysis of primary outcomes

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

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

Trial Site Locations

Total: 1 location

1

Inselspital

Bern, Switzerland, 3010

Actively Recruiting

Loading map...

Research Team

E

Emrush Rexhaj, MD

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

Similar Trials

129Xenon MR Imaging and Spectroscopy Response to Sotatercept...

Pulmonary Hypertension

Actively Recruiting

1 location

An Open-Label, Phase 2 Study Evaluating the Safety of Moslic...

Pulmonary Hypertension

Actively Recruiting

1 location

A Phase 2, Double-blind, Randomized, Placebo-Controlled Stud...

Pulmonary Hypertension

Actively Recruiting

86 locations

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here

Published Research Related To This Trial

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/31175138

The hypertensive disorders of pregnancy: ISSHP classification, diagnosis & management recommendations for international practice.

Mark A Brown, Laura A Magee, Louise C Kenny...

https://pubmed.ncbi.nlm.nih.gov/29803330

Preeclampsia and Cardiovascular Disease in a Large UK Pregnancy Cohort of Linked Electronic Health Records: A CALIBER Study.

Lydia J Leon, Fergus P McCarthy, Kenan Direk...

https://pubmed.ncbi.nlm.nih.gov/31545680

Prevalence of hypertensive disorders during pregnancy in France (2010-2018): The Nationwide CONCEPTION Study.

Valérie Olié, Elodie Moutengou, Clémence Grave...

https://pubmed.ncbi.nlm.nih.gov/34042277