Actively Recruiting
Amino Acid Loss During Continuous Renal Replacement Therapy
Led by Medical University of Vienna · Updated on 2025-05-25
30
Participants Needed
1
Research Sites
94 weeks
Total Duration
On this page
Sponsors
M
Medical University of Vienna
Lead Sponsor
K
Karolinska Institutet
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this observational study is to learn about amino acid loss during continuous renal replacement therapy and plasma amino acid levels in intensive care patients. The main questions it aims to answer are: What amount of amino acids is lost over the duration of continuous renal replacement therapy? How do amino acid plasma concentrations change over time in patients with and without continuous renal replacement therapy? Amino acid concentrations will be measured in the effluent and in the plasma of patients receiving continuous renal replacement therapy as part of their regular medical care. In addition, plasma concentrations of amino acids will be studied in patients without renal replacement therapy.
CONDITIONS
Official Title
Amino Acid Loss During Continuous Renal Replacement Therapy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Postoperative ICU patients
- Age 218 years or older
- Patients receiving enteral or parenteral nutrition as per internal standard procedures
- CRRT treatment planned for CRRT group (including CVVHD, CVVHDF, CVVH types)
- No current or previous (within 30 days) continuous or intermittent renal replacement therapy for non-CRRT group
- No chronic kidney disease stage G3-G5 for non-CRRT group
You will not qualify if you...
- Preoperative intensive care patients
- Patients with liver cirrhosis stage 1-3 according to Child-Pugh classification
- Patients with acute liver failure
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Medical University of Vienna
Vienna, State of Vienna, Austria, 1090
Actively Recruiting
Research Team
S
Sarah Yadavalli, Dr.
CONTACT
A
Arabella Fischer, Dr.
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
2
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