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Dialysis Discussion => Dialysis: General Discussion => Topic started by: okarol on September 23, 2008, 01:07:17 PM
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Comparison of Nocturnal Hemodialysis (NHD) and Short Daily Hemodialysis (DHD) With the NxStage® System One™
This study is currently recruiting participants.
Verified by NxStage Medical, June 2008
Sponsored by: NxStage Medical
Information provided by: NxStage Medical
ClinicalTrials.gov Identifier: NCT00667511
Purpose
The purpose of this study is to determine whether or not nocturnal hemodialysis is equivalent to short daily hemodialysis on a per treatment basis, using the NxStage System One in the home setting.
Condition
Kidney Failure, Chronic
End Stage Renal Disease, Requiring Dialysis
MedlinePlus related topics: Dialysis Kidney Failure
U.S. FDA Resources
Study Type: Observational
Study Design: Case-Only, Prospective
Official Title: Comparison of Nocturnal Hemodialysis (NHD) and Short Daily Hemodialysis (DHD) With the NxStage® System One™
Further study details as provided by NxStage Medical:
Biospecimen Retention: None Retained
Biospecimen Description:
Estimated Enrollment: 30
Study Start Date: April 2008
Estimated Study Completion Date: December 2009
Detailed Description:
End Stage Renal Disease (ESRD) continues to be a devastating clinical condition. The number of patients in 2004 affected by ESRD in the United States rose to 472,000. More than 104,000 new patients began therapy for ESRD in 2004 (1.5% greater than in 2003), while the prevalent dialysis population reached nearly 336,000 (3.4% higher). Total Medicare costs for ESRD in 2004 rose to $20.1 billion while non-Medicare costs rose to $12.4 Billion(1).
Treatment options for ESRD patients are currently limited to either transplantation or dialysis. As daily hemodialysis (DHD) continues to gain widespread acceptance in the dialysis community, there is also renewed interest in nocturnal hemodialysis (NHD) therapy.
NHD has the potential to provide certain advantages over both DHD and conventional thrice-weekly in-center HD. NHD typically consists of 6 - 10 hour treatments while the patient sleeps, providing more gentle fluid removal, more time for equilibration, improved hemodynamic stability and superior clearance of larger solutes(2).
The proposed study plans to explore whether or not NHD is equivalent to DHD on a per treatment basis, using the NxStage System One in the home setting.
1. USRDS 2006 Annual Data Report: Atlas of End-Stage Renal Disease in the United States, NIH, NIDDK, Bethesda, MD, 2006
2. Lacson E, Diaz-Buxo J: Daily and Nocturnal Hemodialysis: How do they stack up? American Journal Kidney Disease, Vol 38(2) Aug 2001: 225-239.
Eligibility
Ages Eligible for Study: 18 Years and older
Genders Eligible for Study: Both
Accepts Healthy Volunteers: No
Sampling Method: Non-Probability Sample
Study Population
Patients must have a stable prescription in the short daily home environment using the NxStage System One prior to enrollment.
Criteria
Inclusion Criteria:
* Patients must have a stable prescription in the short daily home environment using the NxStage System One prior to enrollment.
Exclusion Criteria:
*
Patients are not eligible if:
o they are currently enrolled in another drug or device study which could impact the successful completion of this study
o they are currently on NHD, or less than 3 months since discontinuing NHD
o if they were previously enrolled in this study.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00667511
Locations
United States, California
Satellite Healthcare/Wellbound Recruiting
Mountain View, California, United States, 94041
Contact: Jugjeet Atwal 408-309-5847
Principal Investigator: Brigitte Schiller-Moran, MD
United States, Missouri
Barnes Jewish Dialysis Center Recruiting
St. Louis, Missouri, United States, 63110
Contact: Janet Riley 314-286-0804
Principal Investigator: Brent Miller, MD
United States, Nebraska
Dialysis Center of Lincoln Recruiting
Lincoln, Nebraska, United States, 68512
Contact: Michelle Carver 402-742-8500
Principal Investigator: Leslie Spry, MD
Sub-Investigator: Timothy Govaerts, MD
United States, New York
Rubin Dialysis Recruiting
Saratoga Springs, New York, United States, 12866
Contact: Shari Meola 518-271-0702
Principal Investigator: Christopher Hoy, MD
Principal Investigator: Rachid Daoui, MD
United States, Wisconsin
Commonwealth Dialysis Recruiting
Greenfield, Wisconsin, United States, 53220
Contact: Gail Scott 414-281-6806 gscott@thekidneyinstitute.com
Principal Investigator: William Elliott, MD
Sponsors and Collaborators
NxStage Medical
Investigators
Study Director: Paul Clark NxStage Medical
More Information
Responsible Party: NxStage Medical, Inc. ( Paul Clark, Director of Clinical and Regulatory Affairs )
Study ID Numbers: CP0010
First Received: April 24, 2008
Last Updated: June 23, 2008
ClinicalTrials.gov Identifier: NCT00667511
Health Authority: United States: Food and Drug Administration
Keywords provided by NxStage Medical:
ESRD
End Stage Renal Disease
Daily Hemodialysis
Nocturnal Hemodialysis
Hemodialysis
Kidney Failure
Kidney Disease
Study placed in the following topic categories:
Renal Insufficiency
Urologic Diseases
Renal Insufficiency, Chronic
Kidney Failure, Chronic
Kidney Diseases
Kidney Failure
ClinicalTrials.gov processed this record on September 23, 2008
http://clinicaltrials.gov/ct2/show/NCT00667511
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Thank you for the post we will see if Maggie can get in the trial :thx;