Patient Self-sampling of HPV to Screen for Cervical Cancer

Status Enrolling by invitation

Clinical Trial Summary

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.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05600283
Study type	Interventional
Source	Mayo Clinic
Contact
Status	Enrolling by invitation
Phase	N/A
Start date	November 16, 2022
Completion date	July 30, 2024

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See also
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