Free Fluid Detection With Telementored eFAST
Recruiting
N/A
Interventional Study
Hemoperitoneum
Ascites
Intra-Abdominal Fluid Collection
Postoperative Complications
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Diagnostic
- Participants needed
- 40 (estimated)
- Sponsor
- Oslo University Hospital · Other
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About This Trial
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 …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
Patients who have undergone laparoscopic liver surgery at the Oslo university hospital and are within 72 post-surgery
Exclusion Criteria:
Allergy to ultrasound gel. Patients colonized with ESBL, MRSA and VRE will be excluded due to infection control. Significant postoperative …
Contacts