National cohort study on liver cirrhosis in Switzerland
Official title: SASL Swiss Cirrhosis Cohort Study
Run by University Hospital, Basel, Switzerland · NCT06092385 · Data updated 2026-11-12
This study is tracking patients with liver cirrhosis in Switzerland to gather important information that could help improve treatment and prevent the need for liver transplants.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 3000 (estimated) |
| Sponsor | University Hospital, Basel, Switzerland Academic / other |
| Locations | 10 sites (Lugano, Canton Ticino and 9 other locations) |
| Status | Recruiting |
| Started | June 4, 2024 |
| Main results expected | January 2033 |
| Study ends | January 2033 |
| Registry record updated | July 8, 2025 |
| Trial ID | NCT06092385 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are patients with chronic liver disease who have histologically proven cirrhosis.
✕Probably not a fit
Patients under 18 years old or those who have developed liver cancer will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational cohort study aims to follow patients with liver cirrhosis in Switzerland to collect and analyze a wide range of data, including epidemiological, clinical, histological, psychosocial, and patient-reported outcomes. The study will also biobank biological materials from participants to support future research. By systematically documenting these aspects, the study seeks to understand the disease better and identify potential therapeutic strategies to prevent the need for liver transplantation. The data collected will be used to investigate specific hypotheses related to the progression and management of cirrhosis.
Why it matters
Potential benefit: If successful, this study could lead to improved management strategies for patients with liver cirrhosis, potentially reducing the need for liver transplants.
How similar studies have gone: Other studies focusing on cohort data collection for chronic liver diseases have shown promise, indicating that this approach may yield valuable insights.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * A) Patients with chronic liver disease and histologically proven cirrhosis * B) Control subjects with no signs of cirrhosis Exclusion Criteria: * Age \<18 years * patients who developed hepatocellular carcinoma (HCC) and/or cholangiocellular carcinoma (CCC)
Where it's running
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Gastroenterology and Hepatology, Cantonal Hospital Ticino
Lugano, Canton Ticino, Switzerland Recruiting -
University Centre for Gastrointestinal and Liver Diseases, University Hospital Basel, Switzerland
Basel, Switzerland Recruiting -
Gastroenterology and Hepatology, Lausanne University Hospital
Lausanne, Switzerland Recruiting -
Department of Visceral Surgery and Medicine, University Hospital of Berne
Bern, Switzerland Not yet recruiting -
Gastroenterology and Hepatology, University Hospital Geneva
Geneva, Switzerland Not yet recruiting -
Ticino Liver Centre
Lugano, Switzerland Not yet recruiting
Show 4 more locations
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Gastroenterology and Hepatology, Cantonal Hospital St. Gallen
Sankt Gallen, Switzerland Not yet recruiting -
Arud Centre for addiction medicine Zurich
Zurich, Switzerland Not yet recruiting -
Digestive Diseases Insti- tute GastroZentrum, Hirslanden Clinic Zurich
Zurich, Switzerland Not yet recruiting -
Gastroenterology and Hepatology, University Hospital Zurich
Zurich, Switzerland Not yet recruiting
Study contacts
- Principal investigator: Christine Bernsmeier, Prof. Dr. med. — University Centre for Gastrointestinal and Liver Diseases, University Hospital Basel, Switzerland
- Study coordinator: Christine Bernsmeier, Prof. Dr. med.
- Email: christine.bernsmeier@clarunis.ch
- Phone: +41 61 265 2525
Similar studies
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.