To assess the effect of a probiotic product, when co-administered with antibiotics, on gastrointestinal symptoms following antibiotic treatment in children.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Enrollment
117
Unnamed facility
Warsaw, Poland
Number of loose/watery stools
Time frame: 19-26 days
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.