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Effect of epoetin beta pegol treatment on renal anemia and blood pressure control in non-dialytic CKD patients

Effect of epoetin beta pegol treatment on renal anemia and blood pressure control in non-dialytic CKD patients - Effect of epoetin beta pegol on renal anemia and blood pressure in non-dialytic CKD patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000009449
Enrollment
100
Registered
2013-01-01
Start date
2013-01-04
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

non-dyalitic chronic kidney disease (CKD)

Interventions

Epoetin beta pegol injection to treat renal anemia

Sponsors

Kurashiki Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Chronic kidney disease stage 4 and 5, non-dialytic 2. Hb level lower than 11g/dl 3. Longer than 6 months of therapeutic period estimated until initiation of dialysis 4. Volantary consent obtained after adequate explanation on the study

Exclusion criteria

Exclusion criteria: 1. Allergic to erythropoiesis stimulating agents (ESA) 2. Either malignant diseases, severe infectious diseases, or significant adverse conditions complicated 3. Other inadequate occasions assessed by the attending physician

Design outcomes

Primary

MeasureTime frame
Blood Hb level before and after epoetin beta pegol treatment and mean blood pressure as well as its fluctuation during outpatient clinic.

Secondary

MeasureTime frame
Correlation between blood pressure fluctuation and incidence of cardiovascular events before and after epoetin beta pegol treatment.

Countries

Japan

Contacts

Public ContactKenichiro Asano

Kurashiki Central Hospital Nephrology

ka11734@kchnet.or.jp086-422-0210

Outcome results

None listed

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