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. 2014 Dec 8;2014(12):CD010590. doi: 10.1002/14651858.CD010590.pub2
Methods
  • Study design: RCT

  • Study duration: NS

Participants
  • Setting: University Hospital Ghent

  • Country: Belgium

  • Stage of CKD: kidney transplant recipients

  • Number: epoetin beta (22), no treatment (18)

  • Mean age ± SD (years): epoetin beta (43.5 ± 16.5), no treatment (47.5 ± 16.5)

  • Sex (M/F): epoetin beta (11/11), no treatment (11/7)

  • Other characteristics: NS

  • Exclusion criteria: NS

Interventions Treatment group
  • Epoetin beta

    • SC to target Hb levels of 12.5 g/dL for 3 months


Control group
  • No treatment

    • No treatment


Iron supplementation
  • NS

Outcomes Primary study outcome
  • Hb levels


Outcomes extracted for meta‐analysis
  • Transfusion

Notes
  • Funding: NS

  • Trials registration: not applicable

  • Contact with authors: no record of contact

Risk of bias
Bias Authors' judgement Support for judgement
Random sequence generation (selection bias) Unclear risk Not described
Allocation concealment (selection bias) Unclear risk Not described
Blinding of participants and personnel (performance bias) All outcomes High risk Open label
Blinding of outcome assessment (detection bias) All outcomes Unclear risk Not described
Incomplete outcome data (attrition bias) All outcomes Unclear risk Not described
Selective reporting (reporting bias) High risk Data for cardiovascular events not available
Other bias Low risk None apparent