Suspended
Assessing Cirrhosis Quality of Care While Accounting for Cost: Is the Patient and/or Caregiver Perspective Associated With Outcomes or Quality Metrics, and What is the Cost of Implementing and Measuring Quality Metrics
What is being collected
Data Collection
Collected from today forward - ProspectiveWho is being recruted
Digestive System Diseases+3
+ Fibrosis
+ Liver Cirrhosis
From 18 to 80 Years
+5 Eligibility Criteria
How is the trial designed
Cohort
Tracking disease incidence in order to identify risk factors and understand disease progression over time.Observational
Study Start: December 2017
Summary
Principal SponsorNew York Presbyterian Hospital
Study ContactNicole T Shen, MD
Last updated: January 27, 2026Sourced from a government-validated database.Claim as a partner
Study start date: December 26, 2017
Actual date on which the first participant was enrolled.This study will be conducted using mixed-methods. The qualitative part will consist of in person, 1:1, open ended in depth interviews using a standard interview guide with probes. The quantitative part will document subjects meeting or not meeting the quality metrics supported by strong evidence, clinical outcomes, and medical bills.
Official TitleAssessing Cirrhosis Quality of Care While Accounting for Cost: Is the Patient and/or Caregiver Perspective Associated With Outcomes or Quality Metrics, and What is the Cost of Implementing and Measuring Quality Metrics
Principal SponsorNew York Presbyterian Hospital
Study ContactNicole T Shen, MD
Last updated: January 27, 2026Sourced from a government-validated database.Claim as a partner
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.Design Details
273 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Cohort
These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Conditions
Criteria
Any sex
Biological sex of participants that are eligible to enroll.From 18 to 80 Years
Range of ages for which participants are eligible to join.Conditions
Pathology
Digestive System DiseasesFibrosisLiver CirrhosisLiver DiseasesPathologic ProcessesPathological Conditions, Signs and Symptoms
Criteria
3 inclusion criteria required to participate
primary liver cirrhosis
receiving care at the study cite
no evidence of hepatic encephalopathy if the subject is providing consent
2 exclusion criteria prevent from participating
no documentation of cirrhosis
unable to confirm diagnosis of cirrhosis by imaging or pathology
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Study Objectives
Study Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Recruiting
New York Presbyterian Hospital - Weill Cornell Medicine
New York, United StatesOpen New York Presbyterian Hospital - Weill Cornell Medicine in Google MapsSuspendedOne Study Center