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FREEDOM: Following Rehabilitation, Economics and Everyday-Dialysis Outcome Measurements Study

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City:   Mishawaka
State:   Indiana
Zip Code:   46545
Conditions:   Kidney Failure, Chronic - End Stage Renal Disease, Requiring Dialysis
Purpose:   Purpose The purpose of this study is to compare the economical impact and clinical parameters of short daily hemodialysis using the NxStage® System One hemodialysis device with thrice-weekly conventional in-center dialysis using a matched cohort from the US Renal Data System (USRDS) database.
Study Summary:   In the 21st century, nephrologists in the United States face many challenges including a forecast of decline in physician manpower. Challenges that are specific to hemodialysis (HD) include reimbursement constraints, a growing shortage of nurses and major technological advances in dialysis equipment. There is a growing interest in alternative dialysis regimen and frequency, but a lack of patient incentive for self-care dialysis either in the center or in the home setting. The proposed phase 4 post-marketing study plans to explore whether daily HD is economically attractive compared with thrice weekly HD, while improving health-related quality of life and other dialysis adequacy measures. This project is unique as it provides a large prospective cohort of patients converted to daily HD, with a longitudinal follow up and an ability to compare to a matched cohort from the United States Renal Data Services. This study will help develop whether daily dialysis is economically attractive through the use of new technologies that reduce treatment costs and decrease hospitalization rates, with the long-term hope of increasing life expectancy. All patients will have the option to participate in the Quotidian Dialysis Registry, coordinated by the Lawson Health Research Institute (LHRI) in London, Ontario.
Criteria:   Inclusion Criteria: - Diagnosis of ESRD and require dialysis - Medicare as primary payor (NOTE: Does not include Medicare HMO as primary payer) - Candidate for daily hemodialysis (defined as 6 or more times per week) - Ability to understand and willingness to sign an informed consent statement and a Health Insurance Portability and Accountability Act of 1996 (HIPAA) compliant authorization statement Exclusion Criteria: - Current use of the NxStage System One hemodialysis device - Previous enrollment in this study - Current enrollment in another investigational drug or device trial which might impact the outcome measures planned in this study - Likelihood of not surviving the training period
NCT ID:   NCT00288613
Primary Contact:   Principal Investigator
Bertrand L. Jaber, MD, FASN
Unaffilated

Backup Contact:   N/A
Location Contact:   Mishawaka, Indiana 46545
United States

Cindy Nagy, RN, OCN
Phone: 574-273-6787
Email: cnagy@nephinc.com

Site Status: Recruiting

Data Source:   ClinicalTrials.gov
Date Processed:   May 19, 2013
Modifications to this listing:   Only selected fields are shown, please use the link below to view all information about this clinical trial.
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