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.
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