The goal of this clinical trial is to evaluate anatomical locations for sample collection for future decisions for diagnostic test development.
Study Type
OBSERVATIONAL
Enrollment
234
Mayo Clinic
Rochester, Minnesota, United States
Columbia University
New York, New York, United States
Houston Methodist
Houston, Texas, United States
Number of participants with optimal vaginal samples obtained during the collection process
Number of participants with optimal vaginal samples obtained during the collection process, including preferred anatomical location and yields and quality of samples.
Time frame: 9 months
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