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Clinical Trial Summary

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


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06427200
Study type Interventional
Source Cairo University
Contact
Status Not yet recruiting
Phase Phase 4
Start date July 2024
Completion date July 2027

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