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Evaluation of Blood Loss After Cesarean Delivery Via US Compared to Standard Care

RecruitingNAAges 18 Years - 50 YearsFemaleHoly Family Hospital, Nazareth, Israel
NCT06963047 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

Postpartum hemorrhage and anemia are considered a major health concern due to their impact on maternal morbidity and mortality, quality of life, and maternal cognitive and emotional functioning after delivery, which are particularly important during the critical period of mother-child bonding. Hemoglobin levels in the first 24 hours after delivery do not reflect the lowest point (nadir). The postpartum nadir occurs 48-72 hours after delivery due to the initial redistribution of plasma volume. The aim of this study was to examine whether postpartum ultrasound examination precedes laboratory test results in the diagnosis of anemia due to blood loss after cesarean section.

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📋 Eligibility rules (as published)
Inclusion Criteria: * Women who delivered by a cesarean section. * Age over 18. * Fluent in Hebrew or Arabic. * Signed informed consent form. Exclusion Criteria: * Lack of consent or inability to provide informed consent. * Inability to perform a post-surgical ultrasound, such as post-surgery hospitalization in the intensive care unit. * Women with preoperative coagulation disorders. * Women whose clinical condition requires a post-cesarean ultrasound examination.
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What it tests

  • Ultrasound
  • Standard care
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Where

1 site
Holy family hospital
Nazareth, Israel
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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