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An Observational Study of Hemoglobin Stability in Chronic Kidney Disease Patients on Dialysis Treated With Mircera (Methoxy Polyethylene Glycol-epoetin Beta)

Roche logo

Roche

Status

Completed

Conditions

Anemia

Study type

Observational

Funder types

Industry

Identifiers

NCT01974271
ML28980

Details and patient eligibility

About

This prospective, multicenter, observational study will evaluate the impact of comorbidities on hemoglobin stability in chronic kidney disease patients on dialysis treated with Mircera (methoxy polyethylene glycol-epoetin beta). Eligible patients will be followed for 6 months of treatment.

Enrollment

661 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult patients, >/= 18 years of age
  • Chronic kidney disease patients on hemodialysis or hemodiafiltration for at least 3 months
  • Previously treated with an erythropoietin stimulating agent (ESA)
  • Patient for whom the investigator decided to initiate treatment with Mircera for medical reasons
  • Last hemoglobin level before initiation of Mircera within the range of 10-12 g/dL

Exclusion criteria

  • Current participation in a clinical trial on renal anemia

Trial design

661 participants in 1 patient group

Cohort

Trial contacts and locations

76

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Data sourced from clinicaltrials.gov

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