Clinical Trials Directory

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UnknownNCT03748043

the Effectiveness of Lactoferrin in Treatment of Iron Deficiency Anemia in Children With Chronic Tonsillitis

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
South Valley University · Academic / Other
Sex
All
Age
3 Years – 17 Years
Healthy volunteers
Not accepted

Summary

the investigators will compare the response to iron deficiency anemia to lactoferrin plus ferrous poly maltose versus ferrous poly maltose in Children With Chronic Tonsillitis

Detailed description

Iron deficiency is frequently present with chronic inflammatory disease.(1) Iron deficiency anemia results from decreased body's iron content due to blood loss, poor dietary iron intake, malabsorption, or increased iron requirement. Immune activation drives a diversion of iron to storage sites, particularly the mononuclear phagocytes system in liver and spleen leads to poor hemoglobinization and anemia. Iron deficiency and immune activation lead to disturbances of iron homeostasis.(2) this trial will compare the response to iron deficiency anemia to lactoferrin plus ferrous poly maltose versus ferrous poly maltose in Children With Chronic Tonsillitis

Conditions

Interventions

TypeNameDescription
DRUGLactoferrinlactoferrin 100 mg per day plus ferric hydroxide polymaltose 6 mg /kilogram of Elemental iron
DRUGFerric Hydroxide Polymaltosegroup 2 will receive ferric hydroxide polymaltose 6 mg /kilogram of elemental iron

Timeline

Start date
2019-02-21
Primary completion
2019-05-30
Completion
2019-05-30
First posted
2018-11-20
Last updated
2019-03-19

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT03748043. Inclusion in this directory is not an endorsement.