Prospective Collection of Female Specimens for Testing With Gen-Probe APTIMA (Registered Trademark) Assays
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.
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
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
Conditions
Interventions
- APTIMA® Trichomonas vaginalis & APTIMA® COMBO 2® Assays Device
Device
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
- Dec 31, 2012
- Primary completion
- Jun 30, 2014
- Completion
- Not listed
- Last update posted
- Aug 15, 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 15, 2017 · Synced Jul 25, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT01728103 live on ClinicalTrials.gov.