This study will be conducted to determine the efficacy and safety of lactoferrin versus oral iron versus lactoferrin plus oral iron as an add on therapy in reduced ejection fraction heart failure patients with iron deficiency. •Patients will be randomly distributed into the three groups * All patients will be subjected to baseline data assessment * Follow up after 12 weeks
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
114
oral iron once daily during or after meals as add-on therapy for 12 weeks.
lactoferrin twice daily before meals as add-on therapy for 12 weeks.
lactoferrin twice daily before meals and oral iron once daily during or after meals as add-on therapy for 12 weeks.
Change in health-related quality of life (HR-QoL)
• Change in health-related quality of life (HR-QoL) as evaluated by Minnesota Living with Heart Failure Questionnaire (MLHFQ) minimum score:0 maximum score:105 minimum score is a better outcome
Time frame: 3 months
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