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Completed No phase listed Observational Accepts healthy volunteers

Clinical Evaluation of the APTIMA® HPV Assay Using the PANTHER™ System

ClinicalTrials.gov ID: NCT01446198

Public ClinicalTrials.gov record NCT01446198. 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 5, 2026, 7:34 PM 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 objective is to establish that APTIMA HPV Assay performance on the PANTHER System is comparable to performance on the TIGRIS System.

Study identification

NCT ID
NCT01446198
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Gen-Probe, Incorporated
Industry
Enrollment
11,816 participants

Conditions and interventions

Interventions

Not listed

Eligibility (public fields only)

Age range
18 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
Feb 29, 2012
Primary completion
Apr 30, 2012
Completion
Apr 30, 2012
Last update posted
Jul 2, 2012

2012

United States locations

U.S. sites
3
U.S. states
3
U.S. cities
3
Facility City State ZIP Site status
Gen-Probe Incorporated San Diego California 92121
Hennepin County Medical Center Minneapolis Minnesota 55415
LabCorp Corporation of America Burlington North Carolina 27215

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01446198, 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 Jul 2, 2012 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01446198 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →