Purpose

Probiotics are live microorganisms that, when administered in adequate amounts, confer a health benefit on the host. One of the most common indications for probiotic treatment is the prevention of antibiotic-associated diarrhea (AAD). Unfortunately, many probiotic products used for AAD are not supported by rigorous independent research, and often results in non-evidence-based usage. The overarching objective is to move research forward for the most well-studied Bifidobacterium strain. The primary aim is to test the efficacy of high dose, BB-12-supplemented yogurt in preventing AAD, compared to yogurt without BB-12, in children receiving antibiotics. Other aims are to further assess the safety of yogurt supplemented with BB-12, and to carry out longitudinal community structure and gene expression analysis of fecal microbiota to evaluate the impact of high dose BB-12 in a pediatric population receiving antibiotics. The microbiota includes hundreds of species, and its disruption is hypothesized to be an important factor in the development of AAD.

Condition

Eligibility

Eligible Ages
Between 3 Years and 12 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  1. Child is between ages of 3-12 years 2. Caregiver has the ability to read, speak and write English or Spanish 3. Household has refrigerator for proper storage of drink 4. Household has telephone access 5. Enrollment must take place within 24 hours of starting antibiotics 6. Child was outpatient treated 7. Child was prescribed treatment with a penicillin or cephalosporin class antibiotic regimen for 7-10 days for a respiratory infection; The following is a list (non-exhaustive) of inclusive antibiotics: 1. Amoxicillin 2. Augmentin (amoxicillin/clavulanate) 3. Ancef (cefazolin) 4. Cefadroxil 5. Cephalexin 6. Cephradine 7. Duricef (cefadroxil) 8. Keflex (cephalexin) 9. Kefzol (cefazolin) 10. Velosef (cephradine) 11. Ceclor (cefaclor) 12. Cefotan 13. Cefoxitin 14. Ceftin (cefuroxime) 15. Cefzil (cefprozil) 16. Lorabid (loracarbef) 17. Mefoxin (Cefoxitin) 18. Zinacef (cefuroxime) 19. Omnicef (cefdinir) 20. Suprax (cefixime) 21. Dicloxacillin 22. Pen-Vee K (penicillin)

Exclusion Criteria

  1. Developmental delays 2. Any chronic condition, such as diabetes or asthma, that requires medication 3. Prematurity, or born prior to 37 weeks gestation/of pregnancy 4. Congenital anomalies 5. Failure to thrive 6. Allergy to strawberry 7. Active diarrhea (diarrhea is defined in this study as three or more loose stools per day for two consecutive days) 8. Any other medicines used except anti-pyretic medicines (pro re nata concomitant medications are allowed) 9. Parental belief of lactose intolerance 10. History of heart disease, including valvulopathies or cardiac surgery, any implantable device or prosthetic 11. History of gastrointestinal surgery or disease 12. Milk-protein allergy 13. Allergy to any component of the product or the yogurt vehicle 14. Allergy or a hypersensitivity to the antibiotic prescribed by her/his provider 15. Allergy to any of the following medications: 1. Tetracycline 2. Erythromycin 3. Trimethoprim 4. Ciprofloxacin 16. blood oxygen saturation is less than 90% (if enrollment/baseline visit is completed in person and if the participant was prescribed antibiotics during a telemedicine visit)

Study Design

Phase
Phase 2
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Prevention
Masking
Double (Participant, Investigator)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
BB-12
Bifidobacterium animalis subsp. lactis BB-12 (BB-12)-supplemented yogurt
  • Biological: Bifidobacterium animalis subsp. lactis BB-12
    Bifidobacterium animalis subsp. lactis BB-12-supplemented yogurt
Placebo Comparator
Control
Yogurt without Bifidobacterium animalis subsp. lactis BB-12
  • Other: Control
    Yogurt without Bifidobacterium animalis subsp. lactis BB-12

More Details

Status
Completed
Sponsor
Georgetown University

Study Contact

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.