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Effect of use of test product on vaginal microbiota

Effect of use of test product on vaginal microbiota - Open label test - - Effect of use of test product on vaginal microbiota - Open label test -

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000049695
Enrollment
25
Registered
2022-12-19
Start date
2022-12-19
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy subjects

Interventions

Use test product for 3 days

Sponsors

Miura Clinic, Medical Corporation Kanonkai
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: (1) Subjects of men and women aged 20 to 40 (2) Subjects whose menstrual cycle is around 28 days (3)Subjects who received sufficient explanation about the purpose and content of the test, had the ability to consent, voluntarily volunteered to participate after understanding it well, and agreed to participate in the test in writing

Exclusion criteria

Exclusion criteria: (1) Subjects with a history of diabetes, liver disease, renal disease, gastrointestinal disease, heart disease, respiratory disease, peripheral vascular disease, or other serious disease (2) Subjects with diseases currently being treated (3) Subjects with a history of gynecological disease (endometriosis, uterine fibroids, ovarian cysts, cervical cancer, uterine cancer, etc.) (4) Subjects with food and drug allergies (5) Female subjects who wish to become pregnant while participating in this study, female subjects who are pregnant (including those who may be pregnant) or who are breastfeeding (6) Subjects using products or drugs that affect hormone balance (7) Subjects receiving antibiotics (8) Subjects who participate in strenuous sports and who are on a diet (9)Subjects with irregular lifestyle (10) Subjects who cannot stop taking health foods (including foods for specified health use and foods with functional claims) and quasi-drugs during the test period (11) Subjects who are continuously receiving medical treatment (including OTC and prescription drugs) (12) Subjects who consume alcohol excessively (13) Subjects who cannot abstain from alcohol from the day before the test to the day of the test (14) Subjects participating in or planning to participate in other clinical trials at the start of this study (15) Subjects who are otherwise judged by the principal investigator or subinvestigator to be unsuitable for the study

Design outcomes

Primary

MeasureTime frame
vaginal microbiota

Countries

Japan

Contacts

Public ContactMakoto Terashima

Oneness Support Co., Ltd. Clinical Trial Division

mterashima@oneness-sup.co.jp0648018917

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026