Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
NOT YET RECRUITING
NCT06427200
PHASE4

Efficacy and Safety of Lactoferrin in Heart Failure Patients

Sponsor: Cairo University

View on ClinicalTrials.gov

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

Key Details

Gender

All

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

114

Start Date

2024-07

Completion Date

2027-07

Last Updated

2024-05-24

Healthy Volunteers

No

Interventions

DRUG

oral Iron

oral iron once daily during or after meals as add-on therapy for 12 weeks.

DRUG

Lactoferrin

lactoferrin twice daily before meals as add-on therapy for 12 weeks.

DRUG

lactoferrin and oral iron

lactoferrin twice daily before meals and oral iron once daily during or after meals as add-on therapy for 12 weeks.