Ultrasound for Assessment of Intra-Abdominal Blood Loss After Gynecological Surgery
Recruiting
Observational Study
Post-Operative Hematoma at Operative Site (Diagnosis)
Post-Operative Hemorrhage
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 – 70
- Sex
- Female
- Study type
- Observational
- Participants needed
- 250 (estimated)
- Sponsor
- Holy Family Hospital, Nazareth, Israel · Other
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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, pai…
Trial Locations
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Eligibility Criteria
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 coniza…
Contacts