To assess the tolerability and effect of a probiotic product, when co-administered with antibiotics, on the incidence and duration of loose/watery stools following the antibiotic treatment in children.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Enrollment
400
Multicenter study at 13 health care centers in Warsaw
Warsaw, Poland
Reduction of the incidence of loose/watery stools following antibiotic treatment in children.
Time frame: 19-24 days
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.