Evaluating blood loss after cesarean delivery using ultrasound

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study examines the effectiveness of ultrasound in diagnosing postpartum anemia due to blood loss after cesarean delivery compared to standard care. It focuses on the critical period following delivery, where timely diagnosis and treatment of anemia can significantly impact maternal health and mother-infant bonding. The study aims to determine if ultrasound can provide earlier detection of anemia than traditional laboratory tests, which may not reflect the lowest hemoglobin levels until 48-72 hours postpartum. By addressing postpartum hemorrhage and anemia, the study seeks to improve maternal outcomes and reduce associated risks.

Why it matters

Who can join: the full rules

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.

Where it's running

• Holy family hospital
  Nazareth, North, Israel Recruiting

Study contacts

• Study coordinator: Raed Sa, MD
• Email: r.salim@hfhosp.org
• Phone: +972544986960

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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• Midwife-Led Digital Follow-Up After Cesarean Delivery

  This trial tests whether a midwife-led, four-week digital follow-up after cesarean delivery improves mood, social support, and breastfeeding confidence compared with standard postpartum care.

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• Sleep during the first 48 hours after birth and its link to breastfeeding motivation and success

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• Postpartum acupressure education to support exclusive breastfeeding

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  Recruiting Nigde Omer Halisdemir University · Niğde, Merkez · NCT07410949

How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.