Columbia, Missouri 65201

  • End Stage Renal Disease (ESRD)

Purpose:

The aim of the study is to confirm the safety and clinical effectiveness of Nipro ELISIO-15H and to compare its performance characteristics and hemocompatibility with those of the commercially available dialyzers in U.S.A., Gambro Polyflux Revaclear and Fresenius F160NRe. 10 stable patients will be dialyzed 3 times/week with each dialyzer over 3 weeks. Blood samples for several parameters will be collected during hemodialysis to assess the performance and hemocompatibility of the dialyzers under study. Data thus collected will be analyzed for comparison by standard statistical analysis.


Study summary:

Current patients receiving dialysis treatment for end stage renal disease and who meet the inclusion/exclusion criteria will be entered into the study. These patients will continue on their standard dialysis regimen as stated in the clinics Standard Operating Procedures. Each patient will be studied for three weeks with each week starting with a dialyzer of a different manufacture but of comparable characteristics. Solute clearances and removal will be determined at each of the three dialysis sessions during the week. During session 2 of each week additional specimens will be taken to analyze for hemocompatibility. At the end of the study all clearances and the hemocompatibility markers for each dialyzer will be compared to one another as well as to the manufactures stated characteristics. Blood for the clearance and removal calculations will be taken at time 0, 60 minutes and 240 minutes. Blood for the hemocompatibility determinations will be taken at time 0, 15, 30, 60 and 240 minutes. Flow rates, anticoagulant therapy, erythropoietin therapy, venous and arterial pressures will also be recorded.


Criteria:

Inclusion Criteria: - ESRD patients 18 years or older - Stable on hemodialysis for more than 3 months - Stable hemoglobin between 11-12 g/dl - Stable arteriovenous (AV) fistula vascular access - Stable anticoagulation and ESA regimen - No active infection - Able to sign informed consent and able to participate in the study - Medically stable Exclusion Criteria: - Participation in another study which may interfere with the planned study - Active infection - Medical conditions which may interfere with the study (cardiac, liver disease, Hepatitis) - Allergy to dialyzer membrane materials e.g. polysulfone - Patients which cannot tolerate Heparin - Female who are pregnant or planning to be pregnant - Problem with or allergy to anticoagulation


NCT ID:

NCT02433210


Primary Contact:

Principal Investigator
Madhukar Misra, MD
University of Missouri-Columbia

MADHUKAR MISRA, MD
Phone: 5738827992
Email: misram@health.missouri.edu


Backup Contact:

Email: mooreh@health.missouri.edu
HAROLD MOORE, MA
Phone: 5738824433


Location Contact:

Columbia, Missouri 65201
United States

Maduhkar Misra, MD
Phone: 573-882-7992
Email: misram@health.missouri.edu

Site Status: Recruiting


Data Source: ClinicalTrials.gov

Date Processed: August 03, 2021

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