Skip to content

Antiproteinuric effect of recombinant human erythropoietin (rHuEPO) in predialysis chronic kidney disease (CKD) patients: multicenter observational study

Antiproteinuric effect of recombinant human erythropoietin (rHuEPO) in predialysis chronic kidney disease (CKD) patients: multicenter observational study - Antiproteinuric effect of rHuEPO in predialysis CKD patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000001634
Enrollment
50
Registered
2009-01-14
Start date
2009-01-01
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

Predialysis CKD patients treated with recombinant human erythropoietin (rHuEPO)

Interventions

None listed

Sponsors

Osaka General Medical Center Department of Kidney Disease and Hypertension
Lead Sponsor
Osaka University Hospital
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Outpatients with chronic kidney disease (CKD) who had been examined urinary protein:urinary creatinine ratio for at leaset 3 months before- and after- starting rHuEPO.

Exclusion criteria

Exclusion criteria: Patients with cancer, liver cirrhosis, maintenance dialysis and pregnancy were excluded. Patients who were started or changed with antihypertensives or diuretics or who required admission within 6 months before- and after- rHuEPO initiation.

Design outcomes

Primary

MeasureTime frame
Reduction in proteinuria

Secondary

MeasureTime frame
Correlation between reduction in proteinuria and increase in Hb.

Countries

Japan

Contacts

Public ContactYoshiyuki Furumatsu

Osaka University Graduate School of Medicine Nephrology

furumatsu@yahoo.co.jp06-6879-3857

Outcome results

None listed

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