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

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

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03748043
Enrollment
100
Registered
2018-11-20
Start date
2019-02-21
Completion date
2019-05-30
Last updated
2019-03-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Iron-deficiency

Brief 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

Interventions

DRUGLactoferrin

lactoferrin 100 mg per day plus ferric hydroxide polymaltose 6 mg /kilogram of Elemental iron

DRUGFerric Hydroxide Polymaltose

group 2 will receive ferric hydroxide polymaltose 6 mg /kilogram of elemental iron

Sponsors

South Valley University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
3 Years to 17 Years
Healthy volunteers
No

Inclusion criteria

* children 3-17 years old with chronic tonsillitis

Exclusion criteria

* no other causes of Iron Deficiency Anemia

Design outcomes

Primary

MeasureTime frameDescription
Increase in blood hemoglobin1,3 monthsmean difference in hemoglobin level between pre treatment and post treatment. mean difference in hemoglobin level between pre treatment and post treatment.
Increase in serum ferritin3 monthsmean difference in ferritin level between pre treatment and post treatment.

Countries

Egypt

Contacts

Primary Contactshimaa Ahmed, Lecturer
shimaahaematology@yahoo.com+201064920445

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026