Patients in need of treatment for renal anemia due to ESA administration in patients under On-line HDF treatment
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) The age at the time of acquiring consent is between 20 and 85 years old (2) Renal anemia treatment by ESA administration is under way (3) More than 3 months have passed since On-line HDF implementation (4) ESA has been administered to achieve an anemia improvement target (Hb value of 10 g / dl or more, less than 12 g / dl) continuously for 3 months or more (5) Patient consent was obtained from the patient himself / herself for this research participation
Exclusion criteria
Exclusion criteria: 1) Patients with anemia due to factors other than renal anemia (2) Patients with hypersensitivity to epoetin beta (genetical recombination), darbepoietin alpha (genetical recombination), epoetin beta pegol (genetical recombination) (3) Patients with malignant tumors (4) Pregnant women or patients who may be pregnant, breastfeeding, or who desire pregnancy during research participation (women only) (5) Other Research Responsibilities (In charge) Patients judged by doctors as inappropriate for this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Administration of 30 (30 each) between the three groups of epoetin beta (genetical recombination) group, darbepoietin alpha (genetical recombination) group and epoetin beta pegol (gene recombination) group was administered on-line from the end of on-line HDF Change the target hemoglobin (Hb) maintenance rate and ESA dose during the HDF execution (1 to 2 hours after the start) to examine whether there is an influence due to the change of the ESA administration timing. | — |
Countries
Japan
Contacts
Kaikoukai Medical Foundation Dialysis Medical Division