Free Fluid Detection With Telementored eFAST
Recruiting now · Not applicable
Conditions studied: Hemoperitoneum, Ascites, Intra-Abdominal Fluid Collection, Postoperative Complications
In brief
This feasibility study will evaluate the accuracy of telementored eFAST (Extended Focused Assessment with Sonography in Trauma) in detecting abdominal free fluid in patients who have recently undergone liver surgery. The primary goal is to determine how well the remote-guided ultrasound can identify fluid accumulation compared to conventional ultrasound performed by a radiologist. Participants in this study will be examined with ultrasound, supported in real-time by a remote expert, to assess its accuracy and other relevant performance metrics.
Key facts
- Study ID
- NCT06594562
- Run by
- Oslo University Hospital
- People needed
- 40
- Starts
- 2025-06-18
- Expected to finish
- 2026-10-01
- Last updated by the study team
- 2026-05-15
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients who have undergone laparoscopic liver surgery at the Oslo university hospital and are within 72 post-surgery
You may not qualify if…
- Allergy to ultrasound gel. Patients colonized with ESBL, MRSA and VRE will be excluded due to infection control. Significant postoperative pain that can exacerbated by probe pressure.
Where it is running
- Oslo university hospital, Rikshospitalet — Oslo, Oslo, Norway (enrolling)
Full record on ClinicalTrials.gov
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