Oberhoff 1998.
| Methods | randomized controlled trial, not placebo‐controlled | |
| Participants | n = 227, ovarian, breast, lung, genitourinary, gastrointestinal, other cancer; concomitant treatment: chemotherapy | |
| Interventions | drug = Epoetin beta dose = 5000 IU sc 7x per week hb‐target = 11‐14 g/dL planned ESA duration = 12 weeks |
|
| Outcomes | Primary: transfusion ; secondary: Hb response, safety | |
| Notes | study number = 45434 | |
| Risk of bias | ||
| Bias | Authors' judgement | Support for judgement |
| Adequate sequence generation? | Unclear risk | no description |
| Allocation concealment? | Low risk | central randomization |