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

NCT01446198 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 11816

Last updated 2012-07-03

No results posted yet for this study

Summary

The objective is to establish that APTIMA HPV Assay performance on the PANTHER System is comparable to performance on the TIGRIS System.

Conditions

  • Human Papilloma Virus Infection

Sponsors & Collaborators

  • Gen-Probe, Incorporated

    lead INDUSTRY

Principal Investigators

  • Tadd S Lazarus, M.D. · Gen-Probe, Incorporated

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-03-31
Primary Completion
2012-05-31
Completion
2012-05-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01446198 on ClinicalTrials.gov