Actively Recruiting
Free Fluid Detection With Telementored eFAST
Led by Oslo University Hospital · Updated on 2026-05-07
40
Participants Needed
1
Research Sites
67 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Free Fluid Detection With Telementored eFAST
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients who have undergone laparoscopic liver surgery at the Oslo University Hospital
- Patients within 72 hours after surgery
You will not qualify if you...
- Allergy to ultrasound gel
- Colonization with ESBL, MRSA, or VRE infections
- Significant postoperative pain worsened by probe pressure
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Oslo university hospital, Rikshospitalet
Oslo, Oslo, Norway, 0372
Actively Recruiting
Research Team
P
Peder C Engelsen, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
DIAGNOSTIC
Number of Arms
1
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