O'Shaugnessy 2005.
| Methods | randomized controlled trial, placebo‐controlled | |
| Participants | n = 100, breast cancer (stage I, II, IIIB); concomitant treatment: chemotherapy | |
| Interventions | drug = Epoetin alpha dose = 40000 IU sc weekly hb‐target = 13‐15 g/dL planned ESA duration = during chemotherapy |
|
| Outcomes | Primary: cognitive function, fatigue; secondary: QoL | |
| Notes | study number = 40730 | |
| Risk of bias | ||
| Bias | Authors' judgement | Support for judgement |
| Adequate sequence generation? | Low risk | computer generated |
| Allocation concealment? | Low risk | coded drug packs of identical appearance |