Effects of IV Iron Replacement on Exercise Capacity in Individuals With Heart Failure
Heart Failure, Iron-deficiency
About this trial
This is an interventional treatment trial for Heart Failure focused on measuring Reduced ejection fraction, Exercise, iron supplementation, Cardiopulmonary exercise, peak oxygen uptake
Eligibility Criteria
Inclusion Criteria: Age 18-90 years New York Heart Association Class II-III heart failure Left ventricular dysfunction with left ventricular ejection fraction ≤ 40% Ferritin < 100 ng/mL or 100-300 ng/mL with transferrin saturation (TSAT) < 20% Patients deemed by an attending physician to require intravenous iron therapy The patient is willing and able to comply with the protocol and has provided written informed consent Exclusion Criteria: Iron overload disorders or allergy, concomitant nutritional deficiencies- B12 and folate Recent Acute Coronary Syndrome Physical barriers to exercise capacity Currently presenting in heart failure exacerbation Declined participation Chronic liver disease NYHA class IV Active bleeding Pregnancy Life expectancy ≤ 12 months
Sites / Locations
- Banner - University Medical Center, Phoenix campus
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
IV Iron Infusion Group
Control Group
Subjects will receive iron infusion 1 week after enrollment. Dosage of iron will be at discretion of physicians
Subjects will not receive iron replacement infusion.