ClinicalTrials.Veeva

Menu

Lactoferrin Efficacy Versus Ferrous Sulfate in Treatment of Patients With Iron Deficiency Anemia

A

Assiut University

Status and phase

Completed
Phase 4

Conditions

Iron Deficiency Anemia Treatment

Treatments

Drug: Lactoferrin Bovine
Drug: Ferrous Sulfate

Study type

Interventional

Funder types

Other

Identifiers

NCT04267653
17100915

Details and patient eligibility

About

Lactoferrin (Lf) is a mammalian cationic iron binding glycoprotein belonging to the transferrin family which was discovered 70 years ago, and isolated simultaneously from human and bovine milks in 1960. It is widely distributed in all biological fluids and is also expressed by immune cells, which release it under stimulation by pathogens

Enrollment

96 patients

Sex

All

Ages

2 to 15 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:all patients with iron deficiency anemia from 2 to 15 years old

Exclusion Criteria:

  • Anemia rather than iron deficiency anemia.
  • Family history of blood disease.
  • Patients with thalassemia trait.
  • Patients with chronic illness.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

96 participants in 3 patient groups

lactoferrin
Active Comparator group
Description:
Oral bovine lactoferrin (bfl) 100 mg once daily on empty stomach
Treatment:
Drug: Lactoferrin Bovine
ferrous sulfate
Active Comparator group
Description:
Oral ferrous sulfate 3-6 mg/kg of elemental iron/day in divided doses
Treatment:
Drug: Ferrous Sulfate
combined
Active Comparator group
Description:
combined therapy (both lactoferrin and ferrous sulfate)
Treatment:
Drug: Ferrous Sulfate
Drug: Lactoferrin Bovine

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems