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NCT Number: NCT03218865

Influence of the Vitamine E Coated Dialyzer on Inflammation and Anemia

Evaluation of the effect of a vitamin E coated high flux polysulfone dialyzer on the inflammatory state of patients' end stage renal disease and its clinical benefits in terms of anemia Objectives : To assess the benefits of a vitamin E coated polysulfone membrane on the micro-inflammatory state of chronic dialysis patients Prospective multicenter controlled and randomized study Number of patients : 120 patients (60 patients per group)

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Key information

About this study

Coordinator : Pr JP.CRISTOL Montpellier hospital university Rational : The hemodialyzed patients are subject to inflammation due to their pathologies and to the technique. The VIE dialyzer polysulfon coated to vitamin E has been shown to have a favourable action on inflammation and anemia. The investigators want to highlight the influence of vitamine E graft using as controlled dialyzer a similar polysulfon from the same manufacturer without vitamin E.

Medical device : ViE High flux dialyzer -> vitamin E coated polysulfone membrane manufactured by Asahi Kasei Medical, with CE mark and intended for use in hemodialysis for the patient suffering from acute or chronic renal failure Controlled medical device : Leoceed H high flux dialyzer : polysulfone membrane manufactured by Asahi Kasei Medical, with CE mark and intended for use in hemodialysis for patient suffering from acute or chronic renal failure Objectives : To assess the benefits of a vitamin E coated polysulfone membrane on the micro-inflammatory state of chronic dialysis patients Primary end point : Evolution of the well-known inflammatory marker : High sensibility-CRP Secondary end point : Evolution of the following inflammatory markers : IL-6, TNFa, fibrinogen, antibodies anti- LDLox Evolution of Hemoglobin and ERI Evolution of Nutritional parameters : albumin and pre albumin Study design : Prospective multicenter controlled and randomized protocol study Duration : 12 months Number of patients : 120 patients : 60 patients per group 120 patients : 60 patients per group Adult ESRD patient, whatever the origin, treated by HD, thrice a week for about 4 hours and hemo dynamically well balanced Inclusion criteria : Dialyzed patient on synthetic high flux dialyzer for 3 months Patient with a vascular access allowing a blood flow rate ≥ 250 ml/min Patient with micro inflammation, i.e an average CRP between 5 and 20 mg/L on the two last check-up of CRP Patient informed of the study and having signed the inform consent. Exclusion criteria : Underage patient Subjects who are pregnant or planning to become pregnant during the study Patient with an infection influencing the Hb level

Patient with an Iron deficiency showed with :

Transferin saturation < 20 % and/or Ferritin < 100 µg/L, Hemo transfusion in the last two months Patient treated by HF, HDF, biofiltration Patient with infectious risks Subjects who participated in a clinical study involving dialyzers in the last two months

Criteria of exit :

Patient wish Medical decision Hemo transfusion Departure for another dialysis center Transplantation Death

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult ESRD patient, whatever the origin, treated by HD, thrice a week for about 4 hours and hemo dynamically well balanced
  • Dialyzed patient on synthetic high flux dialyzer for 3 months
  • Patient with a vascular access allowing a blood flow rate ≥ 250 ml/min
  • Patient with micro inflammation, i.e an average CRP between 5 and 20 mg/L on the two last check-up of CRP
  • Patient informed of the study and having signed the inform consent.

Exclusion criteria

  • Underage patient
  • Subjects who are pregnant or planning to become pregnant during the study
  • Patient with an infection influencing the Hb level
  • Patient with an Iron deficiency showed with :

Transferin saturation < 20 % and/or Ferritin < 100 µg/L,

  • Patients having received an Hemo transfusion in the last two months
  • Patient treated by HF, HDF, biofiltration
  • Patient with infectious risks
  • Subjects who participated in a clinical study involving dialyzers in the last two months

Treatment and study plan

VIE high flux dialyzer

Device

Asssesment of the therapeutic effect of the vitamin E coating

Leoceed H high flux dialyzer

Device

Use of the Leoceed H dialyzer during one year per patient enrolled in the control group

Primary outcomes

  1. Evolution of the well-known inflammatory marker : High sensibility-CRP

    Time frame: one year with a follow-up of three months

    Decrease of the CRP marker due the use of vitamin E coated dialyzer

Secondary outcomes

  1. Inflammatory markers

    Time frame: one year with a follow-up of three months

    Evolution of the following inflammatory markers : IL-6, TNFalpha, fibrinogen, antibodies anti-LDLox

  2. Anemia parameters

    Time frame: one year with a follow-up of three months

    Evolution of Hemoglobin and ERI

  3. Nutritional Parameters

    Time frame: one year with a follow-up of three months

    Albumin and pre-albumin parameters

Sponsors and collaborators

Lead sponsor

Hemotech

Industry

Registry information

Official study title

Evaluation of the Dialyzer Vitamin E Coated Effect Inflammatory State of Patients in ESRD and Its Clinical Benefits in Terms of Anemia

Acronym: EVIA

Important dates

Study start
2013
Primary completion
2018
Study completion
2018
First posted
Jul 17, 2017
Registry last updated
Feb 21, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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