Unique ID issued by UMIN | UMIN000012910 |
---|---|
Receipt number | R000015093 |
Scientific Title | A study to evalute iron metabolism by hepcidin-25 in patients on hemodialysis treated with epoetin beta pegol once-monthly or twice--monthly |
Date of disclosure of the study information | 2014/01/21 |
Last modified on | 2014/01/21 15:31:04 |
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
A study to evalute iron metabolism by hepcidin-25 in patients on hemodialysis treated with epoetin beta pegol once-monthly or twice--monthly
Japan |
Renal anemia on hemodialysis patients
Medicine in general | Nephrology |
Others
NO
evaluate iron metabolism by hepcidin-25 in patients on hemodialysis treated with epoetin beta pegol once-monthly or twice-monthly injection
Efficacy
(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
Interventional
Parallel
Randomized
Open -no one is blinded
Dose comparison
2
Treatment
Medicine |
treated epoetin beta pegol once-monthly for one year
treated epoetin beta pegol twice-monthly for one year
20 | years-old | <= |
Not applicable |
Male and Female
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
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
24
1st name | |
Middle name | |
Last name | naohisa tomosugi |
kanazawa medical university medical research institute
Division of Aging Research
daigaku1-1 uchinadamachi kahokugun Ishikawa,Japan
076-286-2211
shogo-k@kanazawa-med.ac.jp
1st name | |
Middle name | |
Last name | Shogo Kimura |
Chuno Kosei Hospital
Division of Nephrology
5-1Wakakusadoori,Seki-city,Gifu
0575-22-2211
shogo-k@kanazawa-med.ac.jp
kanazawa medical university medical research institute,Division of Aging Research
kanazawa medical university medical research institute,Division of Aging Research
Self funding
Chuno Kosei Hospital Division of Nephrology
NO
2014 | Year | 01 | Month | 21 | Day |
Unpublished
No longer recruiting
2013 | Year | 12 | Month | 01 | Day |
2013 | Year | 12 | Month | 01 | Day |
2014 | Year | 01 | Month | 21 | Day |
2014 | Year | 01 | Month | 21 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000015093