Comparison of Conventional Dialysis and the Allient System
Status unconfirmed · Not applicable
Conditions studied: End Stage Renal Disease, Chronic Kidney Failure
In brief
The purpose of the study to determine whether the level of inflammation may be decreased, the lifespan of red blood cells increased and the clearance of waste products in the blood improved through the use of the Allient System as compared to conventional hemodialysis.
Key facts
- Study ID
- NCT00788905
- Run by
- Renal Research Institute
- People needed
- 40
- Starts
- 2008-11-01
- Expected to finish
- 2014-01-01
- Last updated by the study team
- 2013-03-29
Who can join
Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Maintenance in-center hemodialysis
- Age greater than or equal to 18 years
- Has been on hemodialysis for at least 4 months
- Uses a standard single-pass dialysis machine with a high-flux dialyzer
You may not qualify if…
- Hospitalization during the 8 weeks preceding enrollment
- Infection requiring antibiotic treatment during the 8 weeks preceding enrollment
- Central venous cather as dialysis access
- Uncontrollable blood coagulation anomalies
- Smokers
- Dialysis regimen other than 3 times weekly
- In ability to understand the English language and give informed consent for participation in the study
Where it is running
- Irving Place Dialysis Center — New York, New York, United States
- Upper Manhattan Dialysis Center — New York, New York, United States
- Yorkville Dialysis Center — New York, New York, United States
Full record on ClinicalTrials.gov
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