Lung Ultrasound for the Detection of Volume Overload in Patients With Severe Preeclampsia

Recruiting N/A Interventional Study
Pulmonary Edema - Acute Preeclampsia
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Sex
Female
Study type
Interventional
Purpose
Diagnostic
Participants needed
202 (estimated)
Sponsor
Saint Thomas Hospital, Panama · Other
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About This Trial
This research aims to evaluate the usefulness of lung ultrasound (LUS) for detecting and monitoring fluid overload in patients with severe preeclampsia. Severe preeclampsia is a leading cause of maternal death and illness worldwide, often causing fluid buildup that can lead to a serious complication called pulmonary edema, especially after delivery. The study will be a prospective, longitudinal o…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Preeclampsia with severe features. * Gestational age 24 weeks - 41 weeks. Exclusion Criteria: * Chronic lung disease. * Known heart disease. * Diagnosis of lung edema at admission * Body mass index \> 40 * Need for immediate delivery
Contacts

Anna C Figueroa, MD

+507 69494250

annacfigue@gmail.com

CONTACT

Adriana Martinz, MD

amartinzmd@gmail.com

CONTACT