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Completed Not applicable Interventional Accepts healthy volunteers

NeuMoDx PrEDiCTiNG Study Evaluation Plan

ClinicalTrials.gov ID: NCT03970850

Public ClinicalTrials.gov record NCT03970850. 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 20, 2026, 7:44 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

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

Brief summary

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

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).

Study identification

NCT ID
NCT03970850
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
NeuMoDx Molecular, Inc.
Industry
Enrollment
4,017 participants

Conditions and interventions

Interventions

Diagnostic Test

Eligibility (public fields only)

Age range
14 Years to 80 Years
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
Jul 22, 2019 (Actual)
Primary completion
Feb 25, 2020 (Actual)
Completion
Feb 25, 2020 (Actual)
Last update posted
Jun 12, 2020

2019 – 2020

United States locations

U.S. sites
15
U.S. states
10
U.S. cities
15
Facility City State ZIP Site status
University of Alabama Birmingham Alabama 35294 —
Healthcare Clinical Date, Inc. (Segal Trials) North Miami Florida 33161 —
Planned Parenthood - Southwest and Central Florida Orlando Florida 32817 —
Planned Parenthood - Southwest and Central Florida Tampa Florida 33617 —
Indiana University (IU) Indianapolis Indiana 46202 —
LSU Health Science New Orleans Louisiana 70112 —
NeuMoDx Molecular, Inc. Ann Arbor Michigan 48108 —
Henry Ford Health System (HFHS) Detroit Michigan 48202 —
Planned Parenthood - Northern, Central and Southern New Jersey Elizabeth New Jersey 07201 —
Planned Parenthood - Northern, Central and Southern New Jersey Newton New Jersey 07860 —
Planned Parenthood - Northern, Central and Southern New Jersey Riverside Park New Jersey 08075 —
TriCore Reference Labs Albuquerque New Mexico 87505 —
MetroHealth Medical Center Cleveland Ohio 44109 —
Medical University of South Carolina (MUSC) Charleston South Carolina 29425 —
Planned Parenthood - Gulf Coast Houston Texas 77023 —

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 NCT03970850, 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 Jun 12, 2020 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03970850 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →