Clinical Evaluation of the BD Onclarity™ HPV Assay on the BD Viper™ LT

Clinical Trial Summary

The purpose of the study is to compare the results of the Becton Dickinson (BD) Onclarity™ Human Papilloma Virus (HPV) Assay on the BD Viper™ LT instrument from liquid-based cytology (LBC) media diluted in BD HPV LBC diluent to adjudicated histology results from biopsy and a molecular composite comparator.

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NCT number	NCT01944722
Study type	Interventional
Source	Becton, Dickinson and Company
Contact
Status	Completed
Phase	N/A
Start date	August 2013
Completion date	March 2016

Clinical Evaluation of the BD Onclarity™ HPV Assay on the BD Viper™ LT System With Cervical Specimens

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms