Actively Recruiting
Pragmatic Randomized Trial Evaluating CirrhosisRx Clinical Decision Support System on Guideline Adherence and Outcomes for Patients With Cirrhosis
Led by University of California, San Francisco · Updated on 2026-04-01
2106
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the impact of CirrhosisRx, a new clinical decision support (CDS) system, compared to usual care for hospitalized patients with cirrhosis. The study aims to improve adherence to national quality measures and clinical outcomes, addressing the high rates of hospital readmission and mortality among cirrhosis patients. This pragmatic randomized controlled trial uses stepped-wedge cluster randomization of treatment teams to assess the system's effectiveness. Participants receive care either with access to CirrhosisRx, which organizes clinical data and links it to guideline-based order sets for cirrhosis, or with usual care without this system. The trial involves inpatient settings where providers will use or not use the CDS system as assigned. The study focuses on inpatient cirrhosis care and compares groups over time under routine hospital conditions. Throughout approximately 7 days of hospitalization, researchers will monitor adherence to quality measures and clinical outcomes such as inpatient mortality. Data collection includes tracking how well providers follow national guidelines and patient health status during the hospital stay. The study is led by the University of California, San Francisco and follows patients from admission through their hospital course to assess the impact of the CDS system on care quality and outcomes.
CONDITIONS
Brief Title
CirrhosisRx CDS System
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18 years or older
- Diagnosis of cirrhosis based on chronic liver disease and cirrhosis or its complications by ICD-10 codes or clinical documentation
- Currently admitted to the hospital for cirrhosis care at the study institution
You will not qualify if you...
- Children under 18 years old
- Patients who do not meet the cirrhosis diagnosis criteria
- Patients receiving outpatient or ambulatory care rather than inpatient care at the study institution
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Approximately 7 days
Participants receive inpatient care for cirrhosis during which the CirrhosisRx Clinical Decision Support system is used to support guideline adherence or usual care is provided without the system.
1 hospitalization visit (in-person)
Trial Site Locations
Total: 1 location
1
University of California San Francisco Medical Center
San Francisco, California, United States, 94143
Actively Recruiting
Research Team
J
Jin Ge, MD, MBA
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
2
Similar Trials
Frequently Asked Questions
Have more questions? Get in touch with our team for quick support
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here