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Clinical Trial Summary

Evaluation of a novel self-collection device for cervical cancer screening.


Clinical Trial Description

The purpose of this study is to collect design and user input on the safety and effectiveness of the Teal Health self-collection device for patient self-collection of cervicovaginal samples for use with FDA-approved in vitro diagnostics indicated for high risk Human Papillomavirus (hrHPV) screening. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05669911
Study type Interventional
Source Teal Health, Inc.
Contact
Status Active, not recruiting
Phase N/A
Start date August 28, 2022
Completion date December 31, 2023

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