Validation of BD Onclarity™ HPV Assay With PreservCyt® -ASCUS Samples

Status Terminated

Clinical Trial Summary

The purpose of the study is to compare the results of the Becton Dickinson (BD) Human Papilloma Virus (HPV) Assay on the Viper LT instrument from Liquid-based cytology media diluted in HPV diluent to adjudicated histology results from biopsy.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03020121
Study type	Interventional
Source	Becton, Dickinson and Company
Contact
Status	Terminated
Phase	N/A
Start date	November 2016
Completion date	May 2017

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