EligibleTrials

Antiphospholipid Syndrome and Postpartum Pulmonary Artery Pressure

Recruiting · NCT05679206 · Observational (researchers observe without assigning treatment)

View the official record on ClinicalTrials.gov →
Hypertension

Interventions studied

24-hour ambulatory blood pressure monitoringEchocardiography images

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.

Who can take part

Age range
16 Years and older
Sex
Female
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not specified
Study type
Observational (researchers observe without assigning treatment)

Inclusion criteria

Exclusion criteria

Where it is running

1 location listed.

Read the full protocol, contacts and eligibility on ClinicalTrials.gov →

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