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Study identifier: NCT07199998 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Impact of Internal Menstrual Protections on Immunity and Vaginal Microbiota

Condition: Sexual Transmitted Disease · Vaginosis, Bacterial · Mycosis  ·  Sponsor: Centre National de la Recherche Scientifique, France

PhaseN/A
Planned participants300
Who can joinFemale, 18 Years to 49 Years
Healthy volunteersYes

About this study

The availability, effectiveness, and safety of menstrual protection represent a key public health issue. However, research on women's menstrual and sexual health remains extremely limited. Whether societal or pathological, many hypotheses are emerging regarding the effects of menstrual protection products, yet little attention has been given to the products themselves, their societal role, or their physiological and pathological consequences. Internal menstrual products, such as tampons and menstrual cups, are widely used but are subject to limited regulatory oversight, and few studies have investigated their long-term effects on vaginal health. This study aims to investigate how different types of menstrual protection influence vaginal microbiota, immune responses, and the recurrence of gynecological conditions such as bacterial vaginosis, mycosis, or dysbiosis. Biological samples (vaginal, cervical, urinary, and blood) will be collected to analyze vaginal microbiota composition and local immunity. Participants will be divided into three groups based on their main type of menstrual protection: menstrual cup users, tampon users, and external pad users. The study will compare these groups to assess potential differences in vaginal health and immune response related to menstrual product use.

This description comes directly from the study's public registry record.

Talk to the study team

Samuel Alizon, Dr  ·  +33(4)144271667  ·  samuel.alizon@cnrs.fr

Clinical team  ·  cups2@college-de-france.fr

Always discuss trial participation with your own doctor first.

Locations (1)

Institut Alfred FournierParis, Île-de-France Region, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT07199998