Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID05967273

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

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

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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

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