Actively Recruiting
Evaluation of Blood Loss After Cesarean Delivery Via US Compared to Standard Care
Led by Holy Family Hospital, Nazareth, Israel · Updated on 2026-04-13
276
Participants Needed
1
Research Sites
55 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Evaluation of Blood Loss After Cesarean Delivery Via US Compared to Standard Care
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Women who delivered by a cesarean section.
- Age over 18.
- Fluent in Hebrew or Arabic.
- Signed informed consent form.
You will not qualify if you...
- 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.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Holy family hospital
Nazareth, North, Israel
Actively Recruiting
Research Team
R
Raed Sa, MD
CONTACT
B
Bassam Abboud, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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