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Completed No phase listed Observational Accepts healthy volunteers

Prospective Collection of Female and Male Specimens for PANTHER® System Testing

ClinicalTrials.gov ID: NCT01638637

Public ClinicalTrials.gov record NCT01638637. 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 Jul 21, 2026, 4:49 PM EDT

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

Official title

Prospective Collection of Female First-catch Urine, Vaginal Swab, Cervical, and Endocervical Swab Specimens and Male Urethral Swab and First-catch Urine Specimens for Testing With the PANTHER® System

Study identification

NCT ID
NCT01638637
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Gen-Probe, Incorporated
Industry
Enrollment
1,492 participants

Conditions and interventions

Interventions

  • APTIMA Assays; PANTHER System Device

Device

Eligibility (public fields only)

Age range
16 Years and older
Sex
All
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
Jan 31, 2012
Primary completion
May 31, 2013
Completion
Jun 30, 2013
Last update posted
Oct 16, 2013

2012 – 2013

United States locations

U.S. sites
16
U.S. states
14
U.S. cities
16
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35294
Anthony Mills MD Inc. Los Angeles California 90069
Benchmark Research San Francisco California 94102
Planned Parenthood Southern New England New Haven Connecticut 06511
AGA Clinical Trials Hialeah Florida 33012
Wishard Health Services Indianapolis Indiana 46202
Louisiana State University Health Sciences New Orleans Louisiana 70112
John Hopkins University Baltimore Maryland 21205
New England Center for Clinical Research - New Bedford Clinic New Bedford Massachusetts 02744
Hennepin County Medical Center Minneapolis Minnesota 55415
Laboratory Corporation of America Burlington North Carolina 27215
University of North Carolina Chapel Hill Chapel Hill North Carolina 27599-7030
Cincinnati Children's Hospital Medical Center Cincinnati Ohio 45229-3039
Molecular Pathology Laboratory Network, Inc. Maryville Tennessee 37804
Planned Parenthood Houston and Southeast Texas Houston Texas 77023
Tidewater Clinical Research, Inc. -Tidewater Physicians for Women Norfolk Virginia 23502

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 NCT01638637, 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 Oct 16, 2013 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01638637 live on ClinicalTrials.gov.

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