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Terminated No phase listed Observational Accepts healthy volunteers

Prospective Collection of Female Specimens for Testing With Gen-Probe APTIMA (Registered Trademark) Assays

ClinicalTrials.gov ID: NCT01728103

Public ClinicalTrials.gov record NCT01728103. 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 Oct 27, 2026, 2:40 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 for Testing With the APTIMA Assays

Brief summary

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

The objective of this study is to obtain female first-catch urine, vaginal, cervical and endocervical swabs for testing with multiple APTIMA Assays on the Gen-Probe PANTHER® and TIGRIS® Systems.

Study identification

NCT ID
NCT01728103
Recruitment status
Terminated
Study type
Observational
Phase
Not listed
Lead sponsor
Gen-Probe, Incorporated
Industry
Enrollment
1,336 participants

Conditions and interventions

Eligibility (public fields only)

Age range
16 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
Jan 2013 (Type not available)
Primary completion
Jul 2014 (Actual)
Completion
Not listed
Last update posted
Aug 16, 2017

Started 2013

United States locations

U.S. sites
14
U.S. states
14
U.S. cities
14
Facility City State ZIP Site status
Infectious Diseases STD Program University of Alabama at Birmingham Birmingham Alabama 35294 —
Medical Center for Clinical Research San Diego California 92108 —
Healthcare Clinical Data North Miami Florida 33161 —
Mount Vernon Clinical Research Sandy Springs Georgia 30328 —
Louisiana State University Health Sciences Center Dept. of Medicine, Infectious Disease New Orleans Louisiana 70112 —
John Hopkins University Baltimore Maryland 21205 —
New England Center for Clinical Research Fall River Massachusetts 02720 —
University of North Carolina Chapel Hill Chapel Hill North Carolina 27599-7030 —
Cincinnati Children's Hospital Medical Center Division of Pediatric & Adolescent Gynecology Cincinnati Ohio 45229-3039 —
Planned Parenthood Southeastern Pennsylvania Philadelphia Pennsylvania 19107 —
Medical University of South Carolina Charleston South Carolina 29425 —
The Jackson Clinic Jackson Tennessee 38305 —
Planned Parenthood Gulf Coast Houston Texas 77023 —
Tidewater Clinical Research 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 NCT01728103, 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 Aug 16, 2017 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01728103 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →