The aim of the present randomized double-blind placebo-controlled trial is to evaluate the efficacy of a probiotic formulation, containing the probiotic strain Lacticaseibacillus rhamnosus CA15 (DSM 33960), in the treatment of vaginal dysbiosis in terms of: (i) modulation of the microbiota (increase of lactobacilli and decrease of pathogens), (ii) reduction of clinical signs of inflammation, (iii) improvement of quality of life.
Age range
18 Years – 48 Years
Sex
FEMALE
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A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Microbiota
Timeframe: Baseline; end of the treatment (10 days); wash-out (30 days)
Symptomatology
Timeframe: Baseline; end of the treatment (10 days); wash-out (30 days)
Sign
Timeframe: Baseline; end of the treatment (10 days); wash-out (30 days)