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Ultrasound for Assessment of Intra-Abdominal Blood Loss After Gynecological Surgery

Recruitingn/aAges 18 Years - 70 YearsFemaleHoly Family Hospital, Nazareth, Israel
NCT06953141 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

This is a prospective cohort study designed to assess intra-abdominal blood volume and hemodynamic status by measuring the diameter of the inferior vena cava (IVC) using 3D and Doppler ultrasound within 24 hours after gynecological surgery. The study will examine the association between these ultrasound findings and postoperative outcomes, including hemoglobin drop, need for blood transfusion, pain, infection, and length of hospitalization. Approximately 250 women undergoing laparotomy, laparoscopy, or vaginal surgery at Holy Family Hospital will be enrolled. The study also aimed to define postoperative normograms for fluid volume and IVC parameters and to evaluate whether ultrasound-guided decision-making could improve postoperative care and reduce unnecessary interventions.

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📋 Eligibility rules (as published)
Inclusion Criteria: * Women aged 18 years and older * Undergoing gynecological surgery including laparotomy, laparoscopy, and vaginal pelvic surgery * Able to provide informed consent Exclusion Criteria: * Undergoing minor procedures (e.g., dilation and curettage, hysteroscopy, or cervical conization) * Known preoperative coagulation disorders * Postoperative admission to the intensive care unit (ICU) * Clinical indication requiring ultrasound as part of standard postoperative care
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What it tests

  • Ultrasound
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Where

1 site
Holy Family hospital, Nazareth
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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