drugset / Trial / NCT04945707

Impact of Intravenous Iron Repletion On Mechanisms of Exercise InTolerance in HFpEF (IRONMET-HFpEF)

NCT04945707

RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective of this study is to determine if the correction of functional iron deficiency by administering a single dose of intravenous iron (ferric derimaltose or Monoferric®) in participants with heart failure with preserved ejection fraction (HFpEF) will improve exercise capacity as measured by the change in peak oxygen uptake (peak VO2) from baseline to 12 weeks.

Timeline

Start
2021-11-26
Primary completion
2026-06-25
Completion
2026-06-25

Drugs

EvaluationDrugModalityDoseRoute
Comparator Ferric Derisomaltose Unknown 20 mg/kg Intravenous
Comparator Ferric Derisomaltose Unknown 1000 mg Intravenous