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TerminatedNCT02795975Updated Mar 24, 2017

Clinical Evaluation of the Aptima® Combo 2® Assay Using the Panther® System in Female Urine Samples

An observational study in Chlamydia Trachomatis and Gonorrhea, sponsored by Hologic, Inc.. Terminated at 18 sites in United States. Open to female participants aged 14 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2017-03-24.

Sponsored by Hologic, Inc. · Observational

Why this study was terminated
Sponsor business decision
Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
1,766
Ages
14 Years and older
Sex
Female
01

Study summary

The objective of this study is to evaluate the performance characteristics of the AC2 assay on the Panther system using female urine specimens.

02

Conditions studied

  • Chlamydia Trachomatis
  • Gonorrhea

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03

In context

Gonorrhea

155 studies on the registry are indexed under Gonorrhea; 26 are open to participants now.

This study's enrollment of 1,766 is above the median of 451 across 36 observational studies indexed under Gonorrhea.

Browse Gonorrhea studies →

Lead sponsor

Hologic, Inc. is the lead sponsor of 28 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
14 Years and older
Sexes eligible
Female
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Sexually active women ≥14 years of age with or without symptoms of STIs will be eligible for enrollment. Participating clinical collection sites may include US family planning, public health, and STI clinics.

Inclusion criteria

  • The subject is ≥14 years of age at the time of enrollment and is currently sexually active (eg, has had penile/vaginal intercourse within the past 6 months).
  • For subjects under 18 years old, assent of the subject and/or parental/legal guardian permission has been obtained if required by the institutional review board (IRB).
  • The subject and/or legally authorized representative is willing and able to undergo the informed consent process prior to study participation, and:
  • reports symptoms consistent with a suspected STI (eg, abnormal discharge, genital itching, pain/discomfort during sexual intercourse or urination, and/or lower abdominal discomfort); or
  • is asymptomatic and known to be partners with, or a contact of, a person with a confirmed or suspected STI; or
  • is asymptomatic and undergoing screening evaluation for possible STIs; or
  • is asymptomatic and undergoing a routine pelvic examination.

Exclusion criteria

Exclusion Criteria:

  • The subject took antibiotic medications within the last 21 days prior to collection.
  • The subject already participated in the study.
  • The subject has a history of illness that the PI or designee considers could interfere with or affect the conduct, results, and/or completion of the study.
05

Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
1,766 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Sensitivity and specificity

    Time frame: Enrollment ongoing until estimated March 2017

07

Study locations

18 sites
  • The University of Alabama at Birmingham
    Birmingham, Alabama 35294, United States
  • Planned Parenthood of Southern New England, Inc
    New Haven, Connecticut 06511, United States
  • Segal Institute for Clinical Research
    Miami, Florida 33161, United States
  • Eskenazi Hospital - Indiana University School of Medicine
    Indianapolis, Indiana 46202, United States
  • Clinical Trials Management, LLC
    Mandeville, Louisiana 70471, United States
  • Beyer Research
    Kalamazoo, Michigan 49009, United States
  • Quality Clinical Research, Inc.
    Omaha, Nebraska 68114, United States
  • LabCorp
    Burlington, North Carolina 27215, United States
  • University of Cincinnati
    Cincinnati, Ohio 45267, United States
  • University Hospitals Case Medical Center
    Cleveland, Ohio 44106, United States
  • The Ohio State University
    Columbus, Ohio 43210, United States
  • Multnomah County Health Department, STD Clinic
    Portland, Oregon 97204, United States
  • Geneuity
    Maryville, Tennessee 37804, United States
  • Planned Parenthood Gulf Coast, Inc.
    Houston, Texas 77023, United States
  • Brownstone Clinical Trials
    Irving, Texas 75062, United States
  • Clinical Trials of Texas, Inc.
    San Antonio, Texas 78229, United States
  • Tidewater Clinical Research, Inc.
    Virginia Beach, Virginia 23456, United States
  • University of Washington Center for AIDS & STD
    Seattle, Washington 98104, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 24, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02795975
Lead sponsor
Hologic, Inc.
Responsible party
Sponsor
First posted
Jun 10, 2016
Start date
Jun 30, 2016
Primary completion
Mar 1, 2017
Completion
Mar 1, 2017
Last update
Mar 24, 2017

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Mar 2017. You cannot join it, but the record below documents what was studied.

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