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Influence of Probiotics on Prevention of Atopy, Atopic Disease and Immunological Responses

Primary Purpose

Eczema, Asthma, Allergic Rhinitis

Status
Completed
Phase
Phase 2
Locations
Singapore
Study Type
Interventional
Intervention
Probiotics
Placebo
Sponsored by
National University Hospital, Singapore
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Eczema focused on measuring Probiotics, Eczema, Asthma, Allergic Rhinitis, Prevention, Immunological responses

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Parents agree to the subject's participation in the study and informed consent has been obtained. Either parent or sibling (i.e. first degree relative) has a history of atopy. This will be evidenced by a doctor-diagnosis of asthma, allergic rhinitis or eczema and a positive skin prick test to any of a panel of common allergens. The subject is born at above 35 weeks of gestation and weighs above 2 kg. The subject does not have major congenital malformations/major illness. Family appears to be able to successfully complete this trial. Exclusion Criteria: Mother has a medical illness, which in the opinion of the investigator, will interfere with the results of the study. The parent is unable/unwilling to comply with procedures. The parents choose to totally breast-feed the child.

Sites / Locations

  • National University Hospital (NUH)

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Probiotics

Placebo

Arm Description

Bifidobacterium longum [BL999] and Lactobacillus rhamnosus [LPR]

Commercially available cow's milk based infant formula without probiotic supplementation

Outcomes

Primary Outcome Measures

Atopic eczema by 2 years of age

Secondary Outcome Measures

Asthma by 2 years of age
Allergic Rhinitis by 2 years of age
Allergen sensitization by 2 years of age

Full Information

First Posted
April 26, 2006
Last Updated
January 21, 2009
Sponsor
National University Hospital, Singapore
Collaborators
National Medical Research Council (NMRC), Singapore, National University of Singapore
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1. Study Identification

Unique Protocol Identification Number
NCT00318695
Brief Title
Influence of Probiotics on Prevention of Atopy, Atopic Disease and Immunological Responses
Official Title
Influence of Probiotics on Prevention of Atopy, Atopic Disease and Immunological Responses- A Randomized Double-Blind Placebo Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
January 2009
Overall Recruitment Status
Completed
Study Start Date
May 2004 (undefined)
Primary Completion Date
July 2008 (Actual)
Study Completion Date
January 2009 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
National University Hospital, Singapore
Collaborators
National Medical Research Council (NMRC), Singapore, National University of Singapore

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This will be a double-blind, randomized placebo-controlled study. 253 children were recruited and randomly assigned into one of 2 groups to receive either normal infant formula or formula with Bifidobacterium longum and Lactobacillus rhamnosus GG. The primary aim is to assess the effect of early administration (from birth) of probiotics on the incidence of allergic sensitization, eczema, asthma and rhinitis.
Detailed Description
One of the most important early influences on the immune system is the intestinal microflora. The gastrointestinal tract, being the largest body area interacting with the environment, is one of the earliest to be colonized and is quantitatively the most important source of microbial stimulation for the immature immune system. Probiotics are helpful bacteria from healthy intestinal tract, and have shown potential in reducing allergy. This is extremely important as allergic diseases are on the rise worldwide. Probiotics are safe, easy to administer and can be used early for intervention as allergic sensitization, once established, is difficult to reverse. This double-blind, randomized placebo-controlled study has recruited 253 children from birth. These babies, with a family history of atopic disease, will be randomly assigned into one of 2 groups to receive either normal infant formula or formula with Bifidobacterium longum and Lactobacillus rhamnosus GG. The formula will be consumed postnatally for 6 months, after which the child will continue with normal follow-on milk. Children will be examined at the neonatal period and at 1, 3, 6, 12 and 24 months. Blood samples will be collected at birth (cord blood) and at 1 year of age. Blood will be analyzed for cytokines, total IgE and specific IgE. Skin prick test for common allergens will also be performed at 1 year of age. Stools will be collected at 5 days, 1, 3, 12 months and analyzed for the pattern of stool colonization.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Eczema, Asthma, Allergic Rhinitis
Keywords
Probiotics, Eczema, Asthma, Allergic Rhinitis, Prevention, Immunological responses

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
Care ProviderInvestigator
Allocation
Randomized
Enrollment
253 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Probiotics
Arm Type
Experimental
Arm Description
Bifidobacterium longum [BL999] and Lactobacillus rhamnosus [LPR]
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Commercially available cow's milk based infant formula without probiotic supplementation
Intervention Type
Dietary Supplement
Intervention Name(s)
Probiotics
Intervention Description
Bifidobacterium longum [BL999] and Lactobacillus rhamnosus [LPR]
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Commercially available cow's milk based infant formula without probiotic supplementation
Primary Outcome Measure Information:
Title
Atopic eczema by 2 years of age
Secondary Outcome Measure Information:
Title
Asthma by 2 years of age
Title
Allergic Rhinitis by 2 years of age
Title
Allergen sensitization by 2 years of age

10. Eligibility

Sex
All
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Parents agree to the subject's participation in the study and informed consent has been obtained. Either parent or sibling (i.e. first degree relative) has a history of atopy. This will be evidenced by a doctor-diagnosis of asthma, allergic rhinitis or eczema and a positive skin prick test to any of a panel of common allergens. The subject is born at above 35 weeks of gestation and weighs above 2 kg. The subject does not have major congenital malformations/major illness. Family appears to be able to successfully complete this trial. Exclusion Criteria: Mother has a medical illness, which in the opinion of the investigator, will interfere with the results of the study. The parent is unable/unwilling to comply with procedures. The parents choose to totally breast-feed the child.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dr Lynette Shek, Consultant
Organizational Affiliation
National University Hospital (NUH), Singapore
Official's Role
Principal Investigator
Facility Information:
Facility Name
National University Hospital (NUH)
City
Singapore
ZIP/Postal Code
119074
Country
Singapore

12. IPD Sharing Statement

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Influence of Probiotics on Prevention of Atopy, Atopic Disease and Immunological Responses

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