SASL Swiss Cirrhosis Cohort
SASL Swiss Cirrhosis Cohort Study
University Hospital, Basel, Switzerland
3,000 participants
Jun 4, 2024
OBSERVATIONAL
Conditions
Summary
This is a national prospective long-term multicentre observational cohort study following patients with cirrhosis in order to systematically and longitudinally record epidemiological, clinical, histological, psychosocial and patient-reported data and biobank biological material from patients with cirrhosis. The central element of all scientific operation and productivity in the Swiss Cirrhosis Cohort Study (SSCiCoS) is the so-called "nested project" (NP). Based on the evolving large pool of data and biological samples, SSCiCoS investigators use the data pool in order to investigate specific hypotheses and questions.
Eligibility
Inclusion Criteria2
- A) Patients with chronic liver disease and histologically proven cirrhosis
- B) Control subjects with no signs of cirrhosis
Exclusion Criteria2
- Age <18 years
- patients who developed hepatocellular carcinoma (HCC) and/or cholangiocellular carcinoma (CCC)
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Interventions
Clinical assessment and blood sampling at day of inclusion and in 6- monthly intervals for stable cirrhotic patients; at day of inclusion and on days 3, 7, 14 and 28 for acute decompensation or acute-on-chronic liver failure patients; assessment of clinical, psychosocial/behavioural and patient-reported data in parallel with blood sampling; * Biobanking of PBMCs and serum/plasma samples * Biobanking of other biological material if sampled for clinical reasons (liver biopsies, ascites, urine, gut mucosa, lymph nodes)
Locations(10)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06092385