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Study of the SavvyCheck Vaginal Yeast Test

This study is testing a new at-home device called the SavvyCheck Vaginal Yeast Test. This test helps identify if you have a vaginal yeast infection (vulvovaginal candidiasis) by detecting a specific marker from vaginal secretions. Researchers want to see how well this test works when used by individuals like you, compared to the standard lab test (vaginal yeast culture). They will compare the results to understand its accuracy. You may be able to join if you are a woman aged 18 or older and are experiencing symptoms of a vaginal infection, such as increased discharge, itching, or irritation. The study aims to enroll 1200 participants, but its current status is unclear.

Study design
This is an observational study involving 1200 women. It compares the results of a new at-home test to a standard lab test.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
The primary results will be measured at 12 months.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT05079711

Comparative Performance of a Vaginal Yeast Test

Active, Not Recruiting
Not specifiedAges 18+Observational
Uniformed Services University of the Health Sciences
~1,200 participants
Updated 2026-09-10 on ClinicalTrials.gov
What's tested:SavvyCheck Vaginal Yeast Test (rapid, point-of-care diagnostic test)

At a glance

Recruiting sites
0 of 3 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Assess sensitivity and specificity between lay user-performed SavvyCheck Vaginal Yeast Test result compared to the Reference Method (vaginal Candida yeast culture)
Measured over 12 months

Conditions

Vulvovaginal Candidiasis

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Vulvovaginal Candidiasis

NCT05079711

Where you'd take part

This study runs at 3 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Brooke Army Medical Center

    Fort Sam Houston, Texasno site contact published

  • Landstuhl Regional Medical Center

    Landstuhl, Germanyno site contact published

  • Womack Army Medical Center

    Fort Bragg, North Carolinano site contact published

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

Study leadership

  • Elizabeth A Kostas-Polston, PhD · PRINCIPAL_INVESTIGATOR · Uniformed Services University of the Health Sciences

Who to contact

This trial hasn't published a contact. View it on ClinicalTrials.gov

What this trial measures

  • Assess sensitivity and specificity between lay user-performed SavvyCheck Vaginal Yeast Test result compared to the Reference Method (vaginal Candida yeast culture)12 months

    Calculation of sensitivity and specificity of the lay user-performed SavvyCheck Vaginal Yeast Test as compared to the Reference Method (vaginal Candida yeast culture)