Chronic renal failure
Conditions
Interventions
Patients of Group 1 will receive EVAL membrane for 12 months.
Patients of Group 2 will receive vitamin E-coated PS membrane for 12 months.
Sponsors
Yabuki Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Hemodialysis patients who used EVAL membrane more than 3 months prior to study initiation.
Exclusion criteria
Exclusion criteria: Patients who did not agree with participating this clinical study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| hs-CRP, IL-6, events of hypotension during hemodialysis, SPP and baPWV will be measured at 0, 3, 6, 9 and 12 months after study initiation. | — |
Secondary
| Measure | Time frame |
|---|---|
| serum creatinine, serum pre-albumin, serum albumin, muscle volume and BMI will be measured at 0, 3, 6, 9 and 12 months after study initiation. | — |
Countries
Japan
Contacts
Public ContactHayato Nishida
Yamagata University, Faculty of Medicine Department of Urology
Outcome results
None listed