- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06150482
Healthcare Utilization in Liver Cirrhosis Patients, a Multicenter Retrospective Cohort Study
September 25, 2025 updated by: Maastricht University Medical Center
Multicenter, retrospective cohort study investigating healthcare utilization in compensated and decompensated liver cirrhosis patients, including disease course and characteristics associated with healthcare utilization and, for example psychosocial factors.
Study Overview
Study Type
Observational
Enrollment (Estimated)
600
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: B. van Ruijven, MD
- Phone Number: +31631239360
- Email: britt.vanruijven@maastrichtuniversity.nl
Study Locations
-
-
Gelderland
-
Apeldoorn, Gelderland, Netherlands, 7334 DZ
- Recruiting
- Gelre Ziekenhuizen
-
Contact:
- G. Veldhuijzen, MD, PhD
- Phone Number: +31(0)55844 6878
- Email: g.veldhuijzen@gelre.nl
-
-
Limburg
-
Maastricht, Limburg, Netherlands, 6202 AZ
- Recruiting
- Maastricht University Medical Center
-
Contact:
- T.J.G. Gevers, MD, PhD
- Phone Number: +31(0)43-3875021
- Email: tom.gevers@mumc.nl
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Patients with liver cirrhosis
Description
Inclusion Criteria:
- Patients ≥ 18 years of age
- Liver cirrhosis, based on biopsy, fibroscan or diagnostic imaging data
Exclusion Criteria:
- Known malignancy with hepatic metastasis at baseline
- Liver transplantation at baseline
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Number of liver cirrhosis related outpatient contacts before liver cirrhosis complications
Time Frame: 2 years before complication, death or loss to follow-up
|
2 years before complication, death or loss to follow-up
|
|
Number of liver cirrhosis related radiographic imaging before liver cirrhosis complications
Time Frame: 2 years before complication, death or loss to follow-up
|
2 years before complication, death or loss to follow-up
|
|
Number of liver cirrhosis related esophagogastroscopies before liver cirrhosis complications
Time Frame: 2 years before complication, death or loss to follow-up
|
2 years before complication, death or loss to follow-up
|
|
Number of liver cirrhosis related elastographies before liver cirrhosis complications
Time Frame: 2 years before complication, death or loss to follow-up
|
2 years before complication, death or loss to follow-up
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 1, 2022
Primary Completion (Estimated)
December 31, 2026
Study Completion (Estimated)
December 31, 2027
Study Registration Dates
First Submitted
May 23, 2023
First Submitted That Met QC Criteria
November 20, 2023
First Posted (Actual)
November 29, 2023
Study Record Updates
Last Update Posted (Estimated)
September 26, 2025
Last Update Submitted That Met QC Criteria
September 25, 2025
Last Verified
December 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2021-2857-A-2
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.