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NCT04267653 Clinical Trial

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

Iron Deficiency Anemia Treatment Clinical Trial

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

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04267653
Other study ID # 17100915
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date January 1, 2018
Est. completion date October 30, 2018

Study information
Verified date February 2020
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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

Recruitment information / eligibility
Status Completed
Enrollment 96
Est. completion date October 30, 2018
Est. primary completion date January 1, 2018
Accepts healthy volunteers No
Gender All
Age group 2 Years to 15 Years
Eligibility 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.

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Lactoferrin Bovine
treatment for 30 days
• Ferrous Sulfate
treatment for 30 days

Locations
Country Name City State
Egypt AssuitU Assiut

Sponsors (1)
Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary comparison of efficacy of lactoferrin versus ferrous sulfate tharapy in treatment of patients with iron deficiency anemia. Complete blood count will be done before and after therapy to detect the effect of the therapy on serum hemoglobin(g/d) 30 days
Primary Comparison of efficacy of lactoferrin versus ferrous sulfate tharapy in treatment of patients with iron deficiency anemia. Total serum iron(ug/d) will be done before and after therapy to detect effect of the therapy on total serum iron level (ug/d) 30 days
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