NIPH Clinical Trials Search

JAPANESE
国立保健医療科学院
UMIN ID: UMIN000001121

Registered date:22/04/2008

Metabolism of Iron and Erythropoiesis-stimulating agents (ESA) in chronic kidney disease (CKD)

Basic Information

Recruitment status Complete: follow-up continuing
Health condition(s) or Problem(s) studiedCKD (non-dialysis, dialysis)
Date of first enrollment2008/05/01
Target sample size40
Countries of recruitmentJapan
Study typeInterventional
Intervention(s)Treatment with long-acting ESA; dose of ESA and iron were changed by Hb concentration (target 10-11 g/dl). Treatment with traditional ESA; dose of ESA and iron were changed by Hb concentration (target 10-11 g/dl).

Outcome(s)

Primary Outcomemetabolism of iron, oxidative stress, and factors of atherogenesis
Secondary Outcome

Key inclusion & exclusion criteria

Age minimum20years-old
Age maximum90years-old
GenderMale and Female
Include criteria
Exclude criteria1)Malignancy 2)Malnutrition 3)Active inflammatory or infectious disease 4)Uncontrollable diabetes mellitus 5)Abdominal ascites or pleural effusion 6)Pregnancy 7)Inappropriate for this study judged by the physicians

Related Information

Contact

public contact
Name Yukiko Hasuike
Address 1-1 Mukogawa-cho, Nishinomiya, Japan Japan
Telephone 0798-45-6521
E-mail jin@hyo-med.ac.jp
Affiliation Hyogo College of Medicine Department of Internal Medicine, Division of Nephrology and Dialysis
scientific contact
Name Takeshi Nakanishi
Address 1-1 Mukogawa-cho, Nishinomiya, Japan Japan
Telephone 0798-45-6521
E-mail
Affiliation Hyogo College of Medicine Department of Internal Medicine, Division of Nephrology and Dialysis