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Trial record 11 of 38 for:    Recruiting, Not yet recruiting, Available Studies | Chlamydia

NeuMoDx PrEDiCTiNG Study Evaluation Plan

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. Identifier: NCT03970850
Recruitment Status : Not yet recruiting
First Posted : June 3, 2019
Last Update Posted : June 3, 2019
Information provided by (Responsible Party):
NeuMoDx Molecular, Inc.

Brief Summary:
This investigational study will be conducted to evaluate the performance of the NeuMoDx™ CT/NG Assay on the NeuMoDx™ 288 Molecular System and NeuMoDx™ 96 Molecular System (collectively referred to as NeuMoDx™ CT/NG Assay test system).

Condition or disease Intervention/treatment Phase
Chlamydia Trachomatis Infection Neisseria Gonorrheae Infection Diagnostic Test: NeuMoDx CT/NG Assay Diagnostic Test: FDA-cleared NAATs Not Applicable

Detailed Description:

Clinical performance characteristics of the NeuMoDx CT/NG Assay on NeuMoDx™ 288 Molecular System and NeuMoDx™ 96 Molecular System will be evaluated in a multi-center, prospective, sampling study by comparing the diagnoses made by the NeuMoDx™ CT/NG Assay to Patient Infected Status (PIS) as the reference standard.

Prospectively collected urine and swab specimens from individual subjects will be tested using the NeuMoDx™ CT/NG Assay at one of the three NeuMoDx testing sites. Subjects' PIS for CT and PIS for NG will be determined by a central laboratory using FDA-cleared, legally marketed CT/NG combo assays on pre-specified sample matrices according to the PIS determination algorithms.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 3500 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Diagnostic
Official Title: Multi-Center Clinical Performance Evaluation of the NeuMoDx™ Chlamydia Trachomatis (CT) / Neisseria Gonorrhoeae (NG) [CT/NG] Assay on the NeuMoDx™ 288 Molecular System and the NeuMoDx™96 Molecular System
Estimated Study Start Date : July 1, 2019
Estimated Primary Completion Date : December 15, 2019
Estimated Study Completion Date : December 15, 2019

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Gonorrhea

Arm Intervention/treatment
Active Comparator: Multi-arm - Symptomatic and Asymptomatic Males
Arm 1 - Urine from males subjects
Diagnostic Test: NeuMoDx CT/NG Assay
NeuMoDx CT/NG Assay as implemented on NeuMoDx 288 Molecular System and NeuMoDx 96 Molecular System

Active Comparator: Multi-arm - Symptomatic and Asymptomatic Females
Arm 2 - Endocervical, self-collected (in the clinical setting) and physician-collected vaginal swabs and urine from female subjects
Diagnostic Test: NeuMoDx CT/NG Assay
NeuMoDx CT/NG Assay as implemented on NeuMoDx 288 Molecular System and NeuMoDx 96 Molecular System

Active Comparator: Multi-arm - FDA cleared NAATs (Comparator)
Arm 3 - Comparator (for females - vaginal and urine NAATs and for males - 3 urine NAATs)
Diagnostic Test: FDA-cleared NAATs
Testing swabs and urine specimen from both male and female subjects on the FDA-cleared NAATs

Primary Outcome Measures :
  1. Clinical specificity and sensitivity [ Time Frame: Through study completion, an average of 1 year ]
    Clinical specificity and sensitivity of NeuMoDx CT/NG Assay for both CT and NG relative to an individual's patient infected status (PIS)

Secondary Outcome Measures :
  1. Valid results rate [ Time Frame: Through study completion, an average of 1 year ]
    Evaluate indeterminate and unresolved rates

Information from the National Library of Medicine

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Ages Eligible for Study:   14 Years to 80 Years   (Child, Adult, Older Adult)
Sexes Eligible for Study:   All
Gender Based Eligibility:   Yes
Gender Eligibility Description:   Subjects eligible for CT/NG screening (make sure it matches the protocol)
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  1. Male and female subjects of at least 14 years of age or older.
  2. Subject must be able and willing to provide informed consent. The use of a 'surrogate' or 'Legally Authorized Representative' is allowed and shall follow the site's standard procedures, under which the clinical investigation will be conducted.
  3. Subjects undergoing a routine pelvic examination, subjects eligible for screening evaluations for possible STDs and/or subjects known to be partners with a person with a confirmed or suspected STD.
  4. Subject is willing to provide all required specimens.

Exclusion Criteria:

  1. Female subject reports that she had a hysterectomy.
  2. Subject self-reports use of antibiotics within 28 days of study enrollment.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT03970850

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Contact: Nahed Mohsen, PhD 7344770111
Contact: Sundu Brahmasandra, PhD 7344770111

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United States, Alabama
University of Alabama Not yet recruiting
Birmingham, Alabama, United States, 35294
Contact: Barbara Van der Pol   
Principal Investigator: Barbara Van der Pol         
United States, Indiana
Indiana University (IU) Not yet recruiting
Indianapolis, Indiana, United States, 46202
Contact: Becky Buckner   
Principal Investigator: Christopher Emery, MD         
United States, Michigan
NeuMoDx Molecular, Inc. Not yet recruiting
Ann Arbor, Michigan, United States, 48108
Contact: Nahed Mohsen, PhD   
Principal Investigator: Sundu Brahmasandra, PhD         
Henry Ford Health System (HFHS) Not yet recruiting
Detroit, Michigan, United States, 48202
Contact: Kathleen Wilson   
Principal Investigator: Joseph Miller, MD         
United States, New Mexico
TriCore Reference Labs Not yet recruiting
Albuquerque, New Mexico, United States, 87505
Contact: Christine Lente   
Principal Investigator: Steve Young, PhD         
United States, Ohio
MetroHealth Medical Center Not yet recruiting
Cleveland, Ohio, United States, 44109
Contact: Daniel Gebhardt   
Principal Investigator: Ann Avery, MD         
United States, South Carolina
Medical University of South Carolina (MUSC) Not yet recruiting
Charleston, South Carolina, United States, 29425
Contact: Betty Oswald   
Principal Investigator: Gweneth S. Lazenby, MD         
Sponsors and Collaborators
NeuMoDx Molecular, Inc.

Additional Information:
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Responsible Party: NeuMoDx Molecular, Inc. Identifier: NCT03970850     History of Changes
Other Study ID Numbers: CTNG-01-18NMD
First Posted: June 3, 2019    Key Record Dates
Last Update Posted: June 3, 2019
Last Verified: May 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: Yes
Device Product Not Approved or Cleared by U.S. FDA: Yes
Pediatric Postmarket Surveillance of a Device Product: No
Product Manufactured in and Exported from the U.S.: Yes

Additional relevant MeSH terms:
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Chlamydia Infections
Communicable Diseases
Chlamydiaceae Infections
Gram-Negative Bacterial Infections
Bacterial Infections
Sexually Transmitted Diseases, Bacterial
Sexually Transmitted Diseases
Genital Diseases, Male
Genital Diseases, Female
Neisseriaceae Infections