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Clinical Trial Summary

Effect of intravenous iron substitution (iron carboxymaltose (Ferinject®), total dose 15 mg/ kg (maximal dose: 1000mg) in 250 ml 0.9 % NaCl; intravenous infusion in 20 min)in non-anemic premenopausal women with iron deficiency on Primary objective: - Mitochondrial capacity (Phosphocreatine Recovery rate assessed by 31P-MR-spectroscopy of the lower leg muscle) Secondary objectives: - Maximal oxygen uptake during a graded cycling exercise test and time to exhaustion at submaximal power during a constant-load cycling exercise test - Plantarflexor muscle fatiguability as assessed by isokinetic dynamometry - Trial with medicinal product


Clinical Trial Description

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Study Design


Related Conditions & MeSH terms


NCT number NCT01374776
Study type Interventional
Source University of Zurich
Contact
Status Completed
Phase Phase 4
Start date February 2013
Completion date December 2014