Effects of Bifidobacterium Longum BB536 on Incidence of Acute Diarrhea and/or Respiratory- Related Illnesses in Children
Primary Purpose
Healthy Volunteers
Status
Completed
Phase
Not Applicable
Locations
Malaysia
Study Type
Interventional
Intervention
BB536
Placebo
Sponsored by
About this trial
This is an interventional prevention trial for Healthy Volunteers focused on measuring probiotic, children, gastrointestinal, upper respiratory
Eligibility Criteria
Inclusion Criteria:
- Healthy male/ female subjects
- 2-6 years old
- BMI within a healthy range (between 5th to 84th percentile according to children BMI-for-age chart)
- Willing to commit throughout the experiment
Exclusion Criteria:
- Type-1 diabetes
- Long term medication due to certain severe illness
- HIV/AIDS
- Glucose-6-phosphate dehydrogenase (G6PD) deficiency
Sites / Locations
- School of Industrial Technology, Universiti Sains Malaysia
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
BB536
Placebo
Arm Description
Bifidobacterium longum BB536 (9 log CFU/day) and dextrin
100% dextrin
Outcomes
Primary Outcome Measures
Absentia between BB536 vs. Placebo children in daycare centers due to diarrhea and/or respiratory-related illnesses
Severity of diarrhea between BB536 vs. Placebo children
Severity of respiratory-related illnesses between BB536 vs. Placebo children
Secondary Outcome Measures
Fecal microbiota profiles of BB536 vs. Placebo children
Full Information
NCT ID
NCT02434042
First Posted
April 29, 2015
Last Updated
November 2, 2017
Sponsor
Universiti Sains Malaysia
Collaborators
Morinaga Milk Industry Co., LTD
1. Study Identification
Unique Protocol Identification Number
NCT02434042
Brief Title
Effects of Bifidobacterium Longum BB536 on Incidence of Acute Diarrhea and/or Respiratory- Related Illnesses in Children
Official Title
Study on Oral Administration of Bifidobacterium Longum BB536 on Incidence of Acute Diarrhea and/or Respiratory- Related Illnesses Compared to Placebo
Study Type
Interventional
2. Study Status
Record Verification Date
November 2017
Overall Recruitment Status
Completed
Study Start Date
April 1, 2015 (Actual)
Primary Completion Date
February 28, 2016 (Actual)
Study Completion Date
February 28, 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universiti Sains Malaysia
Collaborators
Morinaga Milk Industry Co., LTD
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This project aims to study the benefits of probiotics namely Bifidobacterium longum BB536 in prevention of acute diarrhea and/or respiratory-related illnesses, which are found common among children in Malaysia aged from 2 to 6 years.
Detailed Description
Data from WHO revealed that 5.2 million of children under five of age die every year due to preventable disease such as diarrhea, malaria and pneumonia. In Malaysia, reported cases of diarrhea and acute gastroenteritis have been observed to occur throughout the year, with rotavirus-associated diarrhea being the most prevalently identified gastrointestinal disorder.
Probiotics are preparations of bacteria and yeasts that are considered to confer a beneficial health effect when taken in an adequate amount. Bifidobacterium longum BB536, is a probiotic with over 100 scientific publications based on in vitro, in vivo, and clinical studies, with long consumption history supporting safety and health benefits.
BB536 is also commercially available in Malaysia and Japan in the form of food supplement and health supplements. Some of these include health supplements for children such as MAXBIOTICS, KidsBiotics and JANIPRO BB-G. All these three brands are sold in Malaysia and they all contain mixture of raw ingredient Bifidobacterium longum BB536 manufactured by Morinaga Milk Industry Co., Ltd. and other probiotic strains. In this study, the investigational product, Bifidobacterium longum BB536 and placebo is manufactured by Morinaga Milk Industry Co. Ltd., Japan.
Morinaga BB536 had been awarded FOSHU (Food for Specified Health Uses) status by Japan's Ministry of Health, Labour and Welfare. This status is granted to food products that have been shown in human clinical studies to demonstrate specific health benefits. Also, in year 2007, BB536 had obtained GRAS (Generally Recognised As Safe) certification in USA by FDA. BB536 has confirmed its safety for consumption as it is made in HACCP certified manufacturing plant (Pacific Resources, 2012). BB536 does not contain any porcine or bovine ingredients and has obtained the HALAL certification from the Japan Muslim Association (JMA), Japan. JMA is recognized by JAKIM, Malaysia.
Morinaga B. longum BB536 has been the subject of extensive clinical research and technical development with evidences from more than 100 scientific publications. There are no side effects been reported from the consumption of BB536 including premature infants, pregnant women, elderly people and patients who are taking immunosuppressive drugs. Based on in vitro, in vivo, and clinical studies, long consumption history (more than 30 years) support the safety and health benefits of the strain BB536 by improving intestinal environment, prevention of diarrhea, alleviation of constipation as well as supporting immune system. Based on previous study, ingestion of yogurt fortified with B. longum BB536 can help to reduce harmful bacteria such as Enterobacteriaceae, Streptococcus and C. perfringens, while at the same time alter the microbiota gut profile of volunteers with a significant increase of beneficial microbes Bifidobacterium and Lactobacillus species. Additionally, putrefactive substances in the intestinal environment were also reduced in the presence of the probiotic supplement. There was also clinical trial done on infants in Hidaka General Hospital through the administration of lyophilized powder containing B. longum BB536 and B. breve M-16V each at 9 log cfu/sachet. Such findings suggest that B. longum BB536 is safe and could be used further to evaluate its effect in preventing diarrhea and/or respiratory-related illness prevalence in children from daycare centres.
A total number of five hundred and twenty (520) healthy children from age 2-6 years old will be recruited for this study.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Healthy Volunteers
Keywords
probiotic, children, gastrointestinal, upper respiratory
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
520 (Actual)
8. Arms, Groups, and Interventions
Arm Title
BB536
Arm Type
Active Comparator
Arm Description
Bifidobacterium longum BB536 (9 log CFU/day) and dextrin
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
100% dextrin
Intervention Type
Dietary Supplement
Intervention Name(s)
BB536
Other Intervention Name(s)
Bifidobacterium longum BB536
Intervention Description
Intervention consists of daily administration of 1g probiotic Bifidobacterium longum BB536, administer daily for five days a week at a fixed dosage of 9 log CFU/day for BB536 and continue for 10 months.
Intervention Type
Other
Intervention Name(s)
Placebo
Other Intervention Name(s)
100% dextrin
Intervention Description
Intervention consists of daily administration of 1g of 100% dextrin, administer daily for five days a week and continue for 10 months.
Primary Outcome Measure Information:
Title
Absentia between BB536 vs. Placebo children in daycare centers due to diarrhea and/or respiratory-related illnesses
Time Frame
10 monhts
Title
Severity of diarrhea between BB536 vs. Placebo children
Time Frame
10 months
Title
Severity of respiratory-related illnesses between BB536 vs. Placebo children
Time Frame
10 months
Secondary Outcome Measure Information:
Title
Fecal microbiota profiles of BB536 vs. Placebo children
Time Frame
10 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
6 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Healthy male/ female subjects
2-6 years old
BMI within a healthy range (between 5th to 84th percentile according to children BMI-for-age chart)
Willing to commit throughout the experiment
Exclusion Criteria:
Type-1 diabetes
Long term medication due to certain severe illness
HIV/AIDS
Glucose-6-phosphate dehydrogenase (G6PD) deficiency
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Min Tze Liong, PhD
Organizational Affiliation
Universiti Sains Malaysia
Official's Role
Principal Investigator
Facility Information:
Facility Name
School of Industrial Technology, Universiti Sains Malaysia
City
Pulau Pinang
ZIP/Postal Code
11900
Country
Malaysia
12. IPD Sharing Statement
Learn more about this trial
Effects of Bifidobacterium Longum BB536 on Incidence of Acute Diarrhea and/or Respiratory- Related Illnesses in Children
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