Randomized, Controlled Trial - Lactoferrin Prevention of Diarrhea in Children

Phase

Condition

Colic

Bowel Dysfunction

Hyponatremia

Treatment

N/A

Clinical Study ID

NCT00560222

1R01HD051716-01A2

Ages 12-18
All Genders
Accepts Healthy Volunteers

Study Summary

Much has been learned in recent years about the mechanisms by which breastfeeding improves child health and survival. However, there has been little progress in using these insights to improve pediatric care. Factors that are important for protecting the breast fed infant might be expected to decrease the adverse effects of weaning on diarrhea, growth, and development. The proposed study is meant to begin addressing this important gap by a clinical trial of lactoferrin supplementation in previously weaned children. Lactoferrin,an iron-binding protein with multiple physiological functions (anti-microbial, anti-inflammatory, and immunomodulatory), is one of the most important proteins present in mammalian milk. Our hypothesis is that lactoferrin (given as a daily supplement in amounts similar to those consumed if the child were still breastfed) will improve health by mimicking its protective roles in milk. The significance of these studies is that they will prove feasibility of improving child health after the end of breastfeeding by continuing ingestion of a major protective milk protein. Diarrhea and malnutrition after weaning is a global problem that may be amenable to this approach.

Eligibility Criteria

Inclusion

Inclusion Criteria:

Infants 12 to 18 months of age from the Outpatient clinics (Puestos de Salud) ofDistricto de Independencia in Lima, Peru will be eligible for enrollment in thisstudy.
Infants previously weaned for at least one week will be eligible for study.

Exclusion

Exclusion Criteria:

Infants with either exclusive or partial breast-feeding will not be enrolled; motherswill be encouraged to continue breastfeeding.
Infants ill with severe, persistent or chronic diarrhea will be excluded.
Infants with severe malnutrition (defined as weight-for-height < -3 SDs,height-for-age < -3SDs)will be excluded.
Infants with a serious infections that required hospitalization 1 month prior (e.g.meningitis,pneumonia, bacteremia) will be excluded.
Infants with known HIV (data from parent or medical records) will be excluded.
Infants with underlying chronic illness (e.g. malignancy, immunosuppression, chronicrenal failure, congestive heart failure, liver failure) will be excluded.
Infants with history of allergy to cow's milk or infant formula, eczema, allergicrhinitis or asthma will be excluded.
Infants with a family history of eczema, allergic rhinitis, asthma, or milkintolerance will be excluded.

Study Design

February 01, 2008

October 31, 2011

Study Description

The proposed community-based study will be conducted in a previously weaned population at risk for repeated intestinal infections. Infants who are 12-18 months of age living in the District of Independencia, Lima, Peru will be eligible for enrollment. We will conduct a randomized double blind placebo controlled trial comparing twice daily supplementation with bovine lactoferrin versus a placebo (maltodextrin) Therapy will be continued for 6 months with close monitoring of all study participants for diarrhea and growth.

Specific aim 1: Determine the effect of bovine lactoferrin supplementation on prevention of diarrhea,measured by the number of episodes of diarrhea during a 6 month trial in previously weaned Peruvian children enrolled at 12 to 18 months of age.

Specific aim 2: Determine the effect of bovine lactoferrin supplementation on growth.

Connect with a study center

Universidad Peruana Cayetana Heredia
Lima,
Peru
Site Not Available

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