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Terminated Not applicable Interventional Accepts healthy volunteers

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

ClinicalTrials.gov ID: NCT03020121

Public ClinicalTrials.gov record NCT03020121. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 4, 2026, 12:25 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT03020121
Recruitment status
Terminated
Study type
Interventional
Phase
Not applicable
Lead sponsor
Becton, Dickinson and Company
Industry
Enrollment
28 participants

Conditions and interventions

Interventions

Procedure

Eligibility (public fields only)

Age range
21 Years and older
Sex
Female
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 31, 2016
Primary completion
Apr 30, 2017
Completion
Apr 30, 2017
Last update posted
Jan 30, 2018

2016 – 2017

United States locations

U.S. sites
11
U.S. states
8
U.S. cities
8
Facility City State ZIP Site status
Planned Parenthood of the Rocky Mountains Denver Colorado 80207
American Pathology Partners Inc. Denver Colorado 80222
Comprehensive Clinical Trials, LLC West Palm Beach Florida 33409
Indiana University Indianapolis Indiana 46202
Sidney & Lois Eskenazi Hospital Indianapolis Indiana 46202
Transgenomics Omaha Nebraska 68164
Southwest Womens Health Albuquerque New Mexico 87102
Tricore Reference Lab Albuquerque New Mexico 87102
Research Pathology Associates, LLC Irvington New York 10533
Research Pathology Associates Charlotte North Carolina 22901
Center for Disease Detection San Antonio Texas 78233

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03020121, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 30, 2018 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03020121 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →