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Dysregulation of iron and renal anemia treatment in patients with chronic kidney disease

Dysregulation of iron and renal anemia treatment in patients with chronic kidney disease - DIRAT-2 study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000011949
Enrollment
200
Registered
2013-10-03
Start date
2013-10-07
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

Patients with chronic kidney disease

Interventions

Oral iron supplementation are used in priority to intravenous adminisitration as renal anemia treatment Intravenous iron administration are used as renal anemia treatment

Sponsors

Hyogo College of Medicine
Lead Sponsor
Tanaka-Kitanoda Hospital, Hojo-Tanaka Hospital,Yashiro-Tanaka Clinic
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Chronic kidney disease patients who are administared erythropoiesis stimulating agents (ESA)

Exclusion criteria

Exclusion criteria: malignancy and inflammatory, gastro-intestinal, hepatic, and bone marrow diseases

Design outcomes

Primary

MeasureTime frame
Factors related to iron regulation: serum iron, transferrin saturation rate, ferritin, frataxin et al. Factors related to oxidative stress: malondialdehyde, 8OHdG, AOPP, pentosidine, GSH et al.

Secondary

MeasureTime frame
Factors related to inflammation: high-sensitivity CRP, interleukin-6, tumor necrosis factors-alpha, pentraxin, troponin T, et al. Factors related to nutrition: BMI, albumin, prealbumin et al.

Countries

Japan

Contacts

Public ContactYukiko Hasuike

Hyogo College of Medicine Dep Internal Medicine, Div Kidney and Dialysis

cherry39@hyo-med.ac.jp0798456521

Outcome results

None listed

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