Vaginal Detection of Orally Delivered Probiotic Strains in Healthy Women
ConditionFocus is on Healthy Subjects
Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexFemale
Age18-50
SponsorLallemand Health Solutions
About this trial
The purpose of the present study is to obtain more information on the transit of orally ingested probiotics to the vagina.
Eligibility criteria
Qualifiers
Clinically healthy female between the ages of 18 and 50 years, inclusive,
have a regular or predictable menstrual cycle
Typically have regular bowel movements,
Willing and able to consume a probiotic supplement for 4 weeks,
Disqualifiers
Menopausal women,
Vaginal pH < 2 or > 5 measured at screening,
Women that are lactating, pregnant, attempting to get pregnant, or have a positive pregnancy test,
Use of vaginal probiotics in the last 3 months,
Trial design
Treatments tested in this trial
- Probiotic Formula 1
- Probiotic Formula 2
- Probiotic Formula 3
Treatment groups
72 Participants
are divided into 3 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov