Lactoferrin for Treatment of Iron Deficiency Anemia.

Sponsor
Cairo University (Other)
Overall Status
Completed
CT.gov ID
NCT04435574
Collaborator
(none)
90
1
2
6.8
13.2

Study Details

Study Description

Brief Summary

Anemia is a great public health problem affecting both developing and developed countries. Iron deficiency anemia represents about 50% of causes of anemia worldwide.

Lactoferrin fortified milk has a positive effect on Hb and iron status of infants.

the hypothesis of this study is "lactoferrin may have comparable efficacy to ferrous sulfate therapy with more tolerability and fewer side effects".

the research question of this study is whether oral lactoferrin is effective for treatment of iron deficiency anemia, compared to traditional ferrous sulfate therapy regarding hemoglobin rise and side effects and tolerability.

Condition or Disease Intervention/Treatment Phase
Phase 4

Detailed Description

Anemia is a great public health problem affecting both developing and developed countries. It is considered the most prevalent form of malnutrition in children and adolescents.

Supplementation with standard iron therapy is the main treatment of iron deficiency anemia.

There are two types of iron that are available: ferric and ferrous iron but ferrous iron better in absorption so it is more common in use.

Three types of ferrous iron are present: ferrous sulfate, ferrous fumarate, and ferrous gluconate but all forms have annoying gastrointestinal side effects including diarrhea, anorexia, heartburn, vomiting, nausea, abdominal cramps, upset stomach, and constipation making continuation on it for many weeks unpleasant for all even adults.

Studies have been performed to explore the effect of oral bovine lactoferrin on iron absorption on pregnant women. Many studies showed that oral bovine lactoferrin for pregnant women increased levels of hemoglobin, total serum iron, and ferritin and decreased the prevalence of iron deficiency anemia. although ferrous sulfate and lactoferrin both of them significantly improve the body's iron stores to the same extent, gastrointestinal side effects of lactoferrin were extremely lower than that of ferrous sulfate so oral bovine lactoferrin can replace iron forms in the treatment of iron deficiency anemia in pregnancy.

Lactoferrin is a glycoprotein from the transferrin family consist of 691 amino acids. It is a component of exocrine secretions such as milk and saliva and is present in neutrophil granules. Lactoferrin was identified in 1939 in bovine milk and isolated in 1960 from both human and bovine milk. Human colostrum shows the highest levels of lactoferrin while mature milk and other secretions present lower.

Lactoferrin was used in children as antimicrobial in cases of acute diarrhea.In vitro data document the growth inhibition of the diarrheal associated organisms: rotavirus, cholera, salmonella, and shigella by human lactoferrin.

Studies about Milk formula fortified with bovine lactoferrin confirmed its positive effect on Hb and iron status of infants. Recombinant human lactoferrin was extracted from rice seed, is used by Ventria Bioscience as a dietary supplement for treatment of iron of deficiency anemia.

Rationale:

Iron deficiency anemia has a high prevalence rate in scholar age children with their big need to iron for anabolic processes of growth. Supplementation with standard iron therapy is the main treatment however its unpleasant side effects negatively affect patient compliance.

Hypothesis:

Lactoferrin may have a positive effect in the treatment of iron deficiency anemia in school-age children. Lactoferrin side effects less than standard iron therapy.

Research question:

Is lactoferrin usage in the treatment of iron deficiency anemia in scholar age children has a positive effect and little side effects in comparison with standard iron therapy (ferrous sulfate)?.

  1. Objectives
This study aims to:
  1. Evaluation of the effect of oral lactoferrin in the treatment of iron deficiency anemia in school-age children in comparison with standard iron therapy (ferrous sulfate).

  2. Assessment of side effects occurs with the usage of lactoferrin.

Study Design

Study Type:
Interventional
Actual Enrollment :
90 participants
Allocation:
Randomized
Intervention Model:
Single Group Assignment
Intervention Model Description:
the population for the study will be Scholar age Children attend family medicine clinic for treatment of iron deficiency anemia and their parents accept participation in the study. For confirmation of the diagnosis of iron deficiency anemia the following investigations will be done: CBC Serum total iron full medical history and examination will be performed. study participants will be assigned to either group A (lactoferrin group) or group B (ferrous sulfate group), and will receive the corresponding medication for 8 weeks. 4 weeks follow up for side effects and hemoglobin level and 8 weeks follow up for side effects, hemoglobin level and serum iron will be performed.the population for the study will be Scholar age Children attend family medicine clinic for treatment of iron deficiency anemia and their parents accept participation in the study.For confirmation of the diagnosis of iron deficiency anemia the following investigations will be done:CBC Serum total iron full medical history and examination will be performed. study participants will be assigned to either group A (lactoferrin group) or group B (ferrous sulfate group), and will receive the corresponding medication for 8 weeks. 4 weeks follow up for side effects and hemoglobin level and 8 weeks follow up for side effects, hemoglobin level and serum iron will be performed.
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Comparison of Lactoferrin vs Traditional Iron Therapy for Treatment of Iron Deficiency Anemia in School-age Children.
Actual Study Start Date :
Sep 5, 2018
Actual Primary Completion Date :
Apr 1, 2019
Actual Study Completion Date :
Apr 1, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Group A

group A is lactoferrin group, receiving 100mg sachet of lactoferrin once daily.

Drug: Lactoferrin
Bovine Lactoferrin 100mg sachets.

Active Comparator: Group b

group B is the ferrous sulfate group, receiving 6mg/kg/ day single dose of ferrous sulfate.

Drug: Ferrous Sulfate
6mg/kg of ferrous sulfate.

Outcome Measures

Primary Outcome Measures

  1. Hemoglobin [8 weeks]

    hemoglobin%

  2. Total serum iron [8 weeks]

    Total serum iron

Secondary Outcome Measures

  1. Side effects profile [4 weeks]

    Score of side effects

Eligibility Criteria

Criteria

Ages Eligible for Study:
6 Years to 12 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Children with iron deficiency anemia.
Exclusion Criteria:
  • Malabsorption diseases as coeliac disease.

  • Diseases causing chronic blood loss as Meckel diverticulum.

  • Documented history of allergy to lactoferrin or ferrous sulfate.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Primary care center Giza Egypt 12561

Sponsors and Collaborators

  • Cairo University

Investigators

  • Principal Investigator: Ghada Khfaji, Associate professor, Cairo University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Saeed Salah Abduljalil Soliman, Lecturer of family medicine, Cairo University
ClinicalTrials.gov Identifier:
NCT04435574
Other Study ID Numbers:
  • 70777
First Posted:
Jun 17, 2020
Last Update Posted:
Jun 17, 2020
Last Verified:
Jun 1, 2020
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 17, 2020