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

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00288613
Enrollment
501
Registered
2006-02-08
Start date
2006-01-31
Completion date
2013-11-30
Last updated
2014-07-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

End Stage Renal Disease, Requiring Dialysis, Kidney Failure, Chronic

Keywords

ESRD, Daily Hemodialysis, Hemodialysis, Kidney Failure, Kidney Disease

Brief summary

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.

Detailed description

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.

Interventions

None listed

Sponsors

NxStage Medical
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Hospitalizationsduration of study participationTo compare the all-cause hospitalizations reported in days per patient year on daily hemodialysis using NxStage System One hemodialysis device to thrice-weekly conventional in-center dialysis using a matched cohort from the US Renal Data System (USRDS) database

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026