The objective of this study is to assess the benefit and tolerability of a probiotic product in subjects with increased susceptibility to common cold.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Enrollment
899
A&R
Berlin, Germany
Severity of cold symptoms
Severity of cold symptoms based on the questionnaire WURSS-21 during the cold episodes throughout the study period, in comparison between verum and placebo group
Time frame: 3 months
Incidence of common cold episodes
Time frame: 3 months
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