The purpose of this study is to validate a patient self-sampling vaginal collection kit and laboratory testing for the detection of HPV (human papillomavirus) infection. Researchers will compare the laboratory results of self-collected vaginal swab samples to usual healthcare provider-collected cervical swab samples to determine the laboratory HPV testing accuracy of the self-collection swab.
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Concordance of Patient-collected and Clinician-collected Samples to Detect HPV Infection
Timeframe: Baseline (sample was collected up to 21 days form the date of registration)