Status:
RECRUITING
Ultrasound for Assessment of Intra-Abdominal Blood Loss After Gynecological Surgery
Lead Sponsor:
Holy Family Hospital, Nazareth, Israel
Conditions:
Post-Operative Hematoma at Operative Site (Diagnosis)
Post-Operative Hemorrhage
Eligibility:
FEMALE
18-70 years
Brief Summary
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 with...
Detailed Description
Postoperative intra-abdominal bleeding is a significant contributor to morbidity and, in some cases, mortality following gynecological surgery. Timely recognition of intra-abdominal blood loss is esse...
Eligibility Criteria
Inclusion
- Women aged 18 years and older
- Undergoing gynecological surgery including laparotomy, laparoscopy, and vaginal pelvic surgery
- Able to provide informed consent
Exclusion
- 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
Key Trial Info
Start Date :
May 8 2025
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
July 15 2026
Estimated Enrollment :
250 Patients enrolled
Trial Details
Trial ID
NCT06953141
Start Date
May 8 2025
End Date
July 15 2026
Last Update
May 13 2025
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
Holy Family hospital, Nazareth
Nazareth, Israel