Presepsin as a biomarker of inflammation and prognosis in decompensated liver disease.
Alberto Ferrarese, Mario Plebani, Anna Chiara Frigo...
https://pubmed.ncbi.nlm.nih.gov/33484772/Actively Recruiting
Led by Carol Davila University of Medicine and Pharmacy · Updated on 2024-08-21
30
Participants Needed
1
Research Sites
N/A
Total Duration
Researchers are studying the predictive value of presepsin levels in ascites fluid among patients newly admitted with chronic liver failure. The study focuses on understanding whether presepsin, a fragment of the CD14 receptor involved in detecting bacterial components and triggering inflammation, can help predict outcomes in these patients. Previous studies suggested presepsin in blood may aid early infection diagnosis and mortality prediction in liver cirrhosis, but this study evaluates presepsin directly in ascites fluid. Participants will undergo a diagnostic procedure called paracentesis to collect ascites fluid, where presepsin levels will be measured. This observational study involves patients with chronic liver failure and ascites who meet technical requirements for safe paracentesis. No experimental treatments are given instead, presepsin levels are monitored to assess their relationship with patient outcomes. During the study, participants will be followed for six months to observe mortality and the occurrence of infections, including spontaneous bacterial peritonitis and hepatic encephalopathy. Researchers will collect clinical data and monitor health status regularly to evaluate how presepsin levels in ascites correlate with these outcomes. The study aims to improve prognostic tools for people living with chronic liver failure and ascites.
CONDITIONS
Predictive Values of Presepsin Levels in ASciteS in Patients With Chronic Liver Failure
M
Mihai Ciocirlan
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Carol Davila University of Medicine and Pharmacy
Lead Sponsor
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 day
Participants undergo a diagnostic paracentesis to determine presepsin levels in ascites.
1 visit (in-person)
Duration - 6 months
Participants are monitored for clinical outcomes including mortality, infections, and hepatic encephalopathy.
Follow-up visits as needed over 6 months
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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Alberto Ferrarese, Mario Plebani, Anna Chiara Frigo...
https://pubmed.ncbi.nlm.nih.gov/33484772/Razvan Igna, Irina Gîrleanu, Camelia Cojocariu...
https://pubmed.ncbi.nlm.nih.gov/36143057/Carol Davila University of Medicine and Pharmacy
Lead Sponsor