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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00760851
Other study ID # 2008-01852
Secondary ID
Status Completed
Phase Phase 3
First received September 24, 2008
Last updated March 17, 2011
Start date September 2008
Est. completion date July 2010

Study information

Verified date February 2011
Source Georgetown University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine the effectiveness of probiotics (popularly referred to as 'live active culture' or 'good bacteria') in preventing illnesses and consequent absences from school/daycare centers of children two to four years old that attend daycare at least 3 days per week. Two yogurt drinks will be administered, one containing a specific strain of probiotic, Bb-12. It is hypothesized that children receiving the Bb-12 drink will experience fewer illnesses and absences from daycare.

In this study, participants will be asked to:

1. Give their child 4 oz. of the test yogurt each day for 90 days

2. Keep a daily diary of their child's health

3. Collect 3 stool samples from their child at the start, middle, and end of the study

4. Speak with research personnel on a bi-weekly basis regarding their child's health

5. Ensure that their child to consume any yogurts or probiotic-containing products for 110 days of the study


Recruitment information / eligibility

Status Completed
Enrollment 190
Est. completion date July 2010
Est. primary completion date July 2009
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 2 Years to 4 Years
Eligibility Inclusion Criteria:

- Child aged 2 to 4 years of age

- Child attends daycare at least 3 days per week

Exclusion Criteria:

- Caregiver does not speak English or Spanish

- Caregiver does not agree to have their child refrain from cultured dairy products (yogurt) for the 105-day duration of the study

- Caregiver does not agree to collect a stool sample from their child on Day 0, 45, and 105 of the study

- Caregiver does not have a refrigerator to store the yogurt product at home

- Child is currently receiving breast milk

- Child has an allergy or hypersensitivity to milk proteins or other dairy food components such as lactose

- Child has an allergy or hypersensitivity to strawberry or red food coloring

- Child has a chronic disease

- Child has had an infection or been sick 7 days prior to starting study

- Child has had diarrhea or constipation 7 days prior to starting study

- Child has a special diet as prescribed by a medical professional

- Child has received antibiotics, antiseptics, antifungal, corticosteroids, anti-histamines, non steroidal anti-inflammatory drugs within 7 days prior to starting the study

- Child has a congenital anomaly or birth defect that requires medical care

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention


Intervention

Other:
probiotic strain Bb-12
10^9 CFU Bb-12 per 4 oz yogurt
no Bb-12
yogurt identical to intervention yogurt, only without Bb-12 added.

Locations

Country Name City State
United States Georgetown University Department of Family Medicine, Research Division Washington District of Columbia

Sponsors (3)

Lead Sponsor Collaborator
Georgetown University Penn State University, United States Department of Agriculture (USDA)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary To determine if consumption of a yogurt drink containing Bb-12 decreases the number of absences children have from daycare/school due to illness 90 days No
Secondary Determine if the yogurt supplemented with Bb-12 results in overall improved parental satisfaction due to decreased illnesses in children attending daycare/school 90 No
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