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

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-70
SponsorHoly Family Hospital, Nazareth, Israel

About this trial

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.

Eligibility criteria

Qualifiers

Women aged 18 years and older

Undergoing gynecological surgery including laparotomy, laparoscopy, and vaginal pelvic surgery

Able to provide informed consent

Disqualifiers

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

Trial design

Treatments tested in this trial

  • Ultrasound

Treatment groups

250 Participants
are divided into 1 treatment group