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Procalcitonin in Cirrhotic Patients at High Risk for Sepsis

Role of Procalcitonin (PCT) for the Diagnosis of Sepsis in Ascitic Cirrhotic Patients

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01578226
Enrollment
75
Registered
2012-04-16
Start date
2009-10-31
Completion date
2011-09-30
Last updated
2012-04-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ascites, Cirrhosis, Sepsis

Keywords

Cirrhosis, Ascites, Decompensation, Bacterial infection, Sepsis, Procalcitonin, PCT

Brief summary

Infections are frequent life-threatening events in patients with cirrhosis, occurring at least in 35% of hospitalized patients and accounting for 20% of inpatients death. Among cirrhotics, ascitic patients have the highest risk of death for sepsis. At the admission, no clear-cut clinical and biochemical features are helpful in diagnosing and prognostically stratifying those patients with sepsis. Procalcitonin (PCT)is a breakthrough marker presenting high sensibility and specificity in diagnosing bacterial infections in different clinical settings. The purpose of this study is to evaluate PCT as a diagnostic and prognostic tool for sepsis in hospitalized cirrhotic patients with ascitic decompensation.

Interventions

None listed

Sponsors

Prof. Facchinetti Fabio
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* liver cirrhosis regardless of aetiology * clinically relevant ascitic decompensation at time of hospital admission

Exclusion criteria

* high haematic ascites * ongoing antimicrobial therapy or stopped less than 7 days before admission * last hospital discharge within 7 days * surgery or trauma within 30 days from enrolment * hepatocellular carcinoma out of Milan criteria * extra hepatic malignancies * immunodeficiency syndrome * pregnancy

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026