Clinical Evaluation of the Click Sexual Health Test for the Detection of Neisseria Gonorrhoeae (NG), Trichomonas Vaginalis (TV), and Chlamydia Trachomatis (CT) in Women

Completed

Conditions studied: Chlamydial Infection, Gonococcal Infection, Trichomoniasis

In brief

This study is a multi-center study with a minimum of three CLIA-waived intended operator sites in the United States in which prospectively self-collected vaginal specimens obtained from subjects who are symptomatic or asymptomatic for CT, NG, or TV will be evaluated with the Click Sexual Health Test in a Clinical Laboratory Improvement Amendments (CLIA) waived setting. Subjects interested in participating in this study will be assessed for eligibility and asked to give informed consent and assent, if applicable, by the Investigational Review Board (IRB). Only those subjects who meet the inclusion and exclusion criteria may be enrolled in the study.

Key facts

Study ID

NCT04098900

Run by

Visby Medical

People needed

309

Starts

2019-09-16

Expected to finish

2019-12-03

Last updated by the study team

2020-02-17

Who can join

Age: 14 and older, up to 99. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Willing and able to give voluntary written informed consent and assent form (or the parental/legal guardian will provide parental permission) before any study-related procedure is performed.
• Female at birth. (Pregnant and breastfeeding women are eligible).
• Age greater than or equal to 14 years at the time of enrollment
• Able to read and understand the procedural information provided for the study.
• Able and willing to follow all study procedures, including performing self-collection of one vaginal swab and permitting a HCP to collect three additional vaginal swabs.

You may not qualify if…

• Have a medical condition, serious intercurrent illness, or other circumstance that, in the Investigator's judgement, could jeopardize the subjects's safety, or could interfere with study procedures.
• Enrollment in the DMID 18-0024 and this study previously.
• Use of antiperspirants and deodorants or the following vaginal products: douches, washes, lubricants, vaginal wipes, vaginal moisturizers, or feminine hygiene spray in the genital area, within 48 hours prior to enrollment.

Where it is running

• Therafirst Medical Center — Fort Lauderdale, Florida, United States
• Planned Parenthood North Central States — Saint Paul, Minnesota, United States
• Planned Parenthood of the St. Louis Region and Southwest Missouri — St Louis, Missouri, United States
• Lawrence OB/GYN Clinical Research, LLC — Lawrenceville, New Jersey, United States
• Planned Parenthood Gulf Coast — Houston, Texas, United States

Full record on ClinicalTrials.gov

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