Effect of Lactobacillus Reuteri DSM 17938 to Prevent Antibiotic-associated Diarrhea in Children (PEARL)
Antibiotic Associated Diarrhea
About this trial
This is an interventional prevention trial for Antibiotic Associated Diarrhea focused on measuring Antibiotic associated diarrhea, Children, Prevention, Lactobacillus reuteri DSM 17938, Probiotic
Eligibility Criteria
Inclusion Criteria:
• Children receiving amoxicilline-clavulanic acid (50-90 mg/kg/day, twice daily) due to acute otitis media or acute sinusitis
Exclusion Criteria:
- Receiving antibiotic and/or probiotic, 8 weeks before the study
- Chronic gastrointestinal system disorders
- Congenital anomalies
- Chronic diseases
- Chemotherapy and radiotherapy
- Pregnancy
Sites / Locations
- Sisli Etfal Training and Research Hospital,
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Experimental
Placebo Comparator
Experimental
Placebo Comparator
Study group 1
Study group 2
Study group 3
Study group 4
Amoxicilline-clavulanic acid (50-90 mg/kg/day, twice daily) and Lactobacillus reuteri DSM 17938 (5 drops per day, same time with the first dose of antibiotics). Study Group 1a will received L. reuteri for 10-14 days. Study Group 1b will received L. reuteri for 21 days.
Amoxicillin-clavulanic acid (50-90 mg / kg / day) and placebo ( 5 drops per day, same time with the antibiotics) Study Group 2a will received placebo for 10-14 days. Study Group 2b will received placebo for 21 days.
Amoxicilline-clavulanic acid (50-90 mg/kg/day, twice daily) and Lactobacillus reuteri DSM 17938 (2 x 5 drops per day) Study Group 3a will received L. reuteri for 10-14 days. Study Group 3b will received L. reuteri for 21 days.
Amoxicillin-clavulanic acid (50-90 mg / kg / day) and placebo ( 2 x 5 drops per day, same time with the antibiotics) Study Group 4a will received placebo for 10-14 days. Study Group 4b will received placebo for 21 days.