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Study identifier: NCT06953141 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Post-Operative Hematoma at Operative Site (Diagnosis) · Post-Operative Hemorrhage  ·  Sponsor: Holy Family Hospital, Nazareth, Israel

PhaseN/A
Planned participants250
Who can joinFemale, 18 Years to 70 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Raed Salim, MD  ·  +972544986960  ·  r.salim@hfhosp.org

Reem Younis, MD  ·  +972528328002  ·  reemyounis010@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Holy Family hospital, NazarethNazareth, IsraelRecruiting

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Source record: clinicaltrials.gov/study/NCT06953141