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Terminated NCT04165551

Evaluation of the Consumption of a Probiotic on the Load of S. Agalactiae.

Conditions: Streptococcus Agalactiae

Sex: Female

Ages: 18 Years – 45 Years

Healthy volunteers: Yes

Phase: PHASE1

Enrollment: 3

Sponsor: Biosearch S.A.

Location: Biosearch Life Granada Andalusia

Summary

The objective of this study is to evaluate the effects of oral administration of Lactobacillus BSL\_PS71 on the presence of S. agalactiae in vaginal microbiota of healthy women.

Eligibility Criteria

Inclusion Criteria: * Test positive for S. agalactiae in vaginal exudate * Accept freely to participate in the study and sign the informed consent document Exclusion Criteria: * Consumption of probiotic supplements * Antibiotic use in the period of 2 weeks before the start of the study * Being pregnant or intending to get pregnant in the next 8 weeks * Being allergic to any group of antibiotics

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT04165551). StuddyBuddy aggregates publicly available trial information.