Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
2000 participants
OBSERVATIONAL
2014-07-01
2029-12-31
Brief Summary
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Detailed Description
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After providing informed consent, their demographic, clinical and laboratory / imaging data are uploaded by dedicated study person After discharge from the hospital, follow-up is recommended and uploaded to RH7 (if the follow-up visits take place at this institution \[FDR\]) Mortality data are uploaded from the national registry of dead on regular basis
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Adults with liver cirrhosis admitted to hospital liver unit
Consenting adults admitted with liver cirrhosis; recorded/uploaded are demographic, clinical, laboratory and imaging data
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* decompensating event leading to hospital admission
* informed consent
Exclusion Criteria
19 Years
ALL
No
Sponsors
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F.D. Roosevelt Teaching Hospital with Policlinic Banska Bystrica
OTHER
Responsible Party
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Ľubomír Skladaný MD, PhD
Head, Department of Internal Medicine and HEGITO Liver Unit, Principal Investigator
Principal Investigators
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Lubomir Skladany, MD PhD
Role: PRINCIPAL_INVESTIGATOR
F.D.Roosevelt Teaching Hospital, Banska Bystrica, Slovakia
Locations
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F.D.Roosevelt Teaching Hospital
Banská Bystrica, , Slovakia
Countries
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Central Contacts
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Facility Contacts
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References
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Koller T, Vrbova P, Kubanek N, Zilincanova D, Selcanova SA, Havaj DJ, Skladany L. Assessment of intestinal inflammation via fecal calprotectin for early prediction of adverse outcomes in advanced chronic liver disease. United European Gastroenterol J. 2025 Apr;13(3):305-316. doi: 10.1002/ueg2.12633. Epub 2024 Jul 19.
Other Identifiers
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HEGITO2014
Identifier Type: -
Identifier Source: org_study_id
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