Quirt 1996.
| Methods | randomized controlled trial, placebo‐controlled | |
| Participants | n = 56, lung, gynecological, hematological malignancies, other cancer; concomitant treatment: chemotherapy | |
| Interventions | drug = Epoetin alpha dose = 150 IU/kg sc TIW hb‐target = 12.5‐14 g/dL planned ESA duration = 16 weeks |
|
| Outcomes | Primary: transfusion; secondary: QoL, costs from societal perspective, tumor response | |
| Notes | study number = 80214 | |
| Risk of bias | ||
| Bias | Authors' judgement | Support for judgement |
| Adequate sequence generation? | Unclear risk | no description |
| Allocation concealment? | Unclear risk | no description |