Actively Recruiting
Association Between Venous Excess Ultrasound Grading System and Acute Kidney Injury in the ICU Population
Led by Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) · Updated on 2024-09-05
136
Participants Needed
1
Research Sites
83 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Fluid resuscitation is one of the cornerstones of treatment in ICU patients. Nonetheless, excessive fluid administration can lead to fluid overload which has been associated with worse outcomes in the ICU. To prevent this, assessments of fluid responsiveness are commonly employed. However, fluid responsiveness does not take fluid tolerance into account. Fluid tolerance is the idea that a patient might still be fluid responsive but might already be at risk of the detrimental effects of fluid therapy. Recent developments in point of care ultrasound e.g. the Venous excess ultrasound might help identify patients at risk of fluid overload. However its association with patient relevant outcomes in the ICU remains unclear.
CONDITIONS
Official Title
Association Between Venous Excess Ultrasound Grading System and Acute Kidney Injury in the ICU Population
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients admitted to the ICU who are 18 years or older
- Expected to stay in the ICU for more than 24 hours
You will not qualify if you...
- Obstruction between the right atrium and structures assessed by VExUS
- History of major cardiac shunts (e.g., atrial septal defect)
- History of tricuspid regurgitation
- History of dialysis
- History of portal hypertension
- History of pulmonary hypertension
- History of interstitial lung disease
- Recipients of kidney or liver transplant
- Ultrasound assessment not possible, such as having a BMI over 40
AI-Screening
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Trial Site Locations
Total: 1 location
1
Amsterdam UMC
Amsterdam, North Holland, Netherlands, 1081HV
Actively Recruiting
Research Team
P
Pieter R Tuinman, PhD
CONTACT
P
P Klompmaker, MSc
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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