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N/A N=50

HRQoL in the Low MELD Pre-tx Population

Cirrhosis of the Liver

Enrolled (actual)
50
Serious AEs
0.0%
Results posted
Feb 2014
Primary outcome: Primary: Perceived HRQoL Score. Overall Qualty of Life Index Tool Was Utilized. — 20.19 scores on a scale

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Northwestern University
Primary completion
Jul 2012

Outcome Measures

OutcomeResultp-value
PRIMARY
Perceived HRQoL Score. Overall Qualty of Life Index Tool Was Utilized.
20.19
SECONDARY
Percentage of Subjects With Depressive Scores Who Had a Poor HRQoL
78

Summary

The purpose of this study is to describe the HRQoL in those with MELD scores </= 15 in a single center for those who are pre-liver transplant candidates

Eligibility Criteria

Inclusion Criteria

  • Must be a patient in the liver transplant clinic at Northwestern Memorial Hospital or one of its satellite clinics (including Washington, Illinois; Portage, Indiana; Glenview, Illinois, Oakbrook, Illinois; Joliet, Illinois)
  • Adult patient between the ages of 18-75
  • Ability to read and speak English
  • Must be a candidate for liver transplant per Northwestern Memorial Hospital liver transplant multidisciplinary committee
  • Model for End Stage Liver Disease (MELD) score ≤15
  • Cognitive ability to complete measures

Exclusion Criteria

  • Non-English speaking
  • Those who have already received a liver transplant
  • Hepatic encephalopathy as evidenced by:
  • Grade II or more West Haven Criteria or Adapted West Haven Criteria
  • Evidence of Asterixis upon exam at time of consent (if consented in person)
  • Acute liver failure as etiology for liver disease.
  • MELD score > 15
  • Mental retardation or cognitive disabilities preventing completion of the written questionnaire
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01573325). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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