The purpose of this study is to confirm that treatment with IV ferric carboxymaltose improves exercise capacity, physical functioning and quality of life in patients with iron deficiency and chronic heart failure.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
174
Subjects will receive ferric carboxymaltose intravenously on Day 0, Week 6, and Week 12
Subjects randomised to Standard of Care may receive oral iron at Investigator's discretion however patients will not be permitted to receive IV iron
University Medical Center Groningen
Groningen, Netherlands
Change in Peak VO2 (mL/kg/min) from baseline to Week 24
Time frame: Week 24
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