Longitudinal Clinical Evaluation of the HPV Assay on the BD Viper LT System with Cervical Specimens

  • sponsor
    BD Diagnostics
Updated on 8 November 2020


Longitudinal Clinical Evaluation of the HPV Assay on the BD Viper LT System with Cervical Specimens


The purpose of this study is to evaluate the risk of cervical disease over a period of 3 years and to explore the experimental test as a cervical screening assay. The test results will be compared to the current standards of testing for HPV and diagnosing cervical disease.

Condition Human Papilloma Virus (HPV)
Clinical Study IdentifierTX142570
SponsorBD Diagnostics
Last Modified on8 November 2020


Yes No Not Sure

Inclusion Criteria

Have participated in the Baseline Protocol, BDS-USHPV, and have been identified as eligible for the longitudinal protocol
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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