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A study to evalute iron metabolism by hepcidin-25 in patients on hemodialysis treated with epoetin beta pegol once-monthly or twice--monthly

A study to evalute iron metabolism by hepcidin-25 in patients on hemodialysis treated with epoetin beta pegol once-monthly or twice--monthly - A study to evalute iron metabolism by hepcidin-25 in patients on hemodialysis treated with epoetin beta pegol once-monthly or twice--monthly

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000012910
Enrollment
24
Registered
2014-01-21
Start date
2013-12-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Renal anemia on hemodialysis patients

Interventions

treated epoetin beta pegol once-monthly for one year treated epoetin beta pegol twice-monthly for one year

Sponsors

kanazawa medical university medical research institute,Division of Aging Research
Lead Sponsor
Chuno Kosei Hospital Division of Nephrology
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.patients who receive three times a week of hemodialysis more than three months 2.patients treated with 50-200 CERA per month 3.patients who hemoglobin density of 3 months undergoes a change of at 10-12 g/dL in the past 4.patients that clear iron lack is not accepted in the past three months (Ferritin over 50 ng/mL) 5.20 years old or older 6.patients who acccept this study

Exclusion criteria

Exclusion criteria: 1.patients who do not accept this study 2.patients who have allergy for ESA 3.patients who have uncontrollable high blood pressure 4.patients with factors that could have a clear impact on hemoglobin concentration, such as infectious diseases, malignant tumors, bleeding of moderate or more 5.women who are pregnant,breastfeeding,possibly pregnant,or not willing to use birth control in the period leading up to the end of the study at the time of obtaining informed consent 6.patients who received red bllod cell transfusion within 3 months before enrollment 7.patients who are judged ineligible by the physician in charge

Design outcomes

Primary

MeasureTime frame
(1) biological parameters of iron metabolism(including Hep-25) (2) ERI(ESA Resistance Index) at endpoint (3) pecentage of maintaing the target Hb level for one year

Countries

Japan

Contacts

Public ContactShogo Kimura

Chuno Kosei Hospital Division of Nephrology

shogo-k@kanazawa-med.ac.jp0575-22-2211

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026