None (Healthy subjects)
Conditions
Interventions
Ingestion of dairy ingredient for 12 weeks
Ingestion of placebo for 12 weeks
Sponsors
Bunkyo Garden Women's Clinic
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1)Female subjects 2)Subjects between 50 to 65 years old 3)More than 1 year has passed since the last menstrual period
Exclusion criteria
Exclusion criteria: 1)Subjects diagnosed with bacterial vaginosis within the past 3 months 2)Subjects with Nugent score of 7 or higher 3)Subjects who have received oral or intravenous antibiotic treatment within the past 3 months from the time of screening 4)Subjects who plan to make major lifestyle changes (diet, sleep, exercise, etc.) during the study period 5)Subjects having a milk allergy 6)Subjects who regularly consume foods containing a dairy ingredient to be evaluated 7)Subjects who have serious disease in the liver, kidney heart, lung, gastrointestinal tract, blood, endocrine system, or metabolic system etc. Or those who have serious medical history of these 8)Subjects who have medical history of drug allergy or severe food allergy 9)Others who have been determined as ineligible for the research subject of this study, judging by the principal investigator on the findings of their background, physical observations, physical examination, and so on
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Nugent score | — |
Secondary
| Measure | Time frame |
|---|---|
| Nugent subscore | — |
Countries
Japan
Contacts
Public ContactTamaki Furuhata
EP Mediate Co., Ltd. Development Department Trial Planning Section
Outcome results
None listed