Comparative Performance of the SavvyCheck Vaginal Yeast Test Versus Culture

Status: Recruiting
Location: See all (3) locations...
Intervention Type: Device
Study Type: Observational
SUMMARY

The purpose of this study is to establish lay user performance criteria for the SavvyCheck Vaginal Yeast Test in comparison to standard vaginal yeast culture and identification method for Candida (the Reference Method). Polymerase chain reaction (PCR) and sequencing of fungi will be used as an aid to explain the nature of the discrepancy in the case of discordant results between the lay user-performed SavvyCheck Vaginal Yeast Test and standard vaginal yeast culture and identification method for Candida.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: t
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⁃ Symptomatic Women Symptomatic women include those women who present with a complaint consistent with symptoms of vaginitis (e.g., increased vaginal discharge, vaginal itching, vaginal soreness and irritation, rash on the labia, and genital burning that may worsen during urination). Enrollment will continue at each clinical site until our target number of 216 Reference Method (vaginal Candida yeast culture) positives have been collected. We estimate up to 600 symptomatic women will be enrolled to meet our target.

• DoD Military Health System beneficiary

• Have a healthcare appointment at a recruitment clinic

• 18 years of age or older

• Must speak and understand English

• Able to provide informed consent

• Women experiencing vaginal symptoms, including: increased discharge, itching, soreness and irritation, rash on the labia, and genital burning that may worsen during urination

• Must determine the test is applicable to her based on her symptoms after she has read the outside device labeling (box label)

⁃ Asymptomatic Women Asymptomatic women include those women who do not present with a complaint consistent with vaginitis. Enrollment will continue at each clinical site until our target number of 170 Reference Method (vaginal Candida yeast culture) negatives have been collected. We estimate up to 320 asymptomatic women will be enrolled to meet our target.

• DoD Military Health System beneficiary

• Have a healthcare appointment at a recruitment clinic

• 18 years of age or older

• Must speak and understand English

• Able to provide informed consent

• Healthy women appearing for routine care without symptoms of vaginal yeast infection

Locations
United States
North Carolina
Womack Army Medical Center
RECRUITING
Fort Bragg
Texas
Brooke Army Medical Center
NOT_YET_RECRUITING
Fort Sam Houston
Other Locations
Germany
Landstuhl Regional Medical Center
RECRUITING
Landstuhl
Contact Information
Primary
Elizabeth A Kostas-Polston, PhD
elizabeth.kostas-polston@usuhs.edu
301.295.1531
Backup
Mary B Engler, PhD
mary.engler@usuhs.edu
301.295.3427
Time Frame
Start Date: 2022-03-18
Estimated Completion Date: 2026-08-30
Participants
Target number of participants: 1200
Treatments
Symptomatic for vaginal yeast
Women presenting to the clinic with symptoms of vulvovaginal candidiasis.
Asymptomatic for vaginal yeast
Women presenting to the clinic with no symptoms of vulvovaginal candidiasis.
Related Therapeutic Areas
Sponsors
Leads: Uniformed Services University of the Health Sciences
Collaborators: Savvyon Diagnostics Ltd.

This content was sourced from clinicaltrials.gov