Assessment of intestinal inflammation via fecal calprotectin for early prediction of adverse outcomes in advanced chronic liver disease.
Tomas Koller, Petra Vrbova, Natalia Kubanek...
https://pubmed.ncbi.nlm.nih.gov/39031494Actively Recruiting
Led by F.D. Roosevelt Teaching Hospital with Policlinic Banska Bystrica · Updated on 2022-08-03
2000
Participants Needed
1
Research Sites
464 weeks
Total Duration
Researchers are collecting detailed information from adult patients hospitalized with liver cirrhosis at a specialized liver unit. The study aims to track the frequency and types of liver cirrhosis complications, such as decompensation events, and measure mortality rates over one year. This observational registry helps to better understand the clinical course and outcomes of liver cirrhosis in hospitalized adults. Upon hospital admission, consenting adults diagnosed primarily with liver cirrhosis and experiencing a decompensating event are enrolled. Their demographic details, clinical status, laboratory tests, and imaging results are carefully recorded and uploaded to the study database. After discharge, follow-up information is collected when patients return to the same institution, and mortality information is regularly updated from the national death registry. Participants provide informed consent and contribute data during hospitalization and follow-up visits. Researchers monitor clinical changes, frailty status at admission, and survival outcomes at 90 days and one year. The total duration of participation varies depending on follow-up visits and outcomes. This registry supports ongoing observation of liver cirrhosis progression and associated health events in adults.
CONDITIONS
Cirrhosis Registry of Hospitalized Patients
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Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person) at hospital admission
Duration - Up to 1 year
Participants who undergo routine care are observed with their demographic, clinical, laboratory, and imaging data collected during hospitalization and follow-up.
Follow-up visits as part of routine care, with data uploaded if visits occur at the hospital
Total: 1 location
1
F.D.Roosevelt Teaching Hospital
Banská Bystrica, Slovakia, 97401
Actively Recruiting
L
Lubomir Skladany, MD, PhD
J
Janka Vnencakova, PhD
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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Tomas Koller, Petra Vrbova, Natalia Kubanek...
https://pubmed.ncbi.nlm.nih.gov/39031494