drugset / Trial / NCT06427200

Efficacy and Safety of Lactoferrin in Heart Failure Patients

NCT06427200

Phase 4 Not yet recruiting 114 enrolled Cairo University
RandomizedParallel-groupOpen-labelTreatment

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

Timeline

Start
2024-07
Primary completion
2027-07
Completion
2027-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Iron Sulfate Small molecule Oral
Subject Lactoferrin Protein / enzyme biologic