Actively Recruiting

Age: 18Years - 70Years
FEMALE
NCT06953141

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

Led by Holy Family Hospital, Nazareth, Israel · Updated on 2026-04-13

250

Participants Needed

1

Research Sites

83 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years - 70Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Women aged 18 years and older
  • Undergoing gynecological surgery including laparotomy, laparoscopy, and vaginal pelvic surgery
  • Able to provide informed consent
Not Eligible

You will not qualify if you...

  • Undergoing minor procedures such as 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

AI-Screening

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Trial Site Locations

Total: 1 location

1

Holy Family hospital, Nazareth

Nazareth, Israel

Actively Recruiting

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Research Team

R

Raed Salim, MD

CONTACT

R

Reem Younis, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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