Clinical trial Recruiting at 3 sites Observational Ages 18 and up

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.

More Liver Cirrhosis trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment3000 (estimated)
SponsorUniversity Hospital, Basel, Switzerland
Academic / other
Locations10 sites (Lugano, Canton Ticino and 9 other locations)
StatusRecruiting
StartedJune 4, 2024
Main results expectedJanuary 2033
Study endsJanuary 2033
Registry record updatedJuly 8, 2025
Trial IDNCT06092385 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

  • 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
  • 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

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.