Clinical Evaluation of the ID NOW™ CT/NG Test
Status unconfirmed · Not applicable
Conditions studied: Chlamydia Trachomatis Infection, Neisseria Gonorrheae Infection, Asymptomatic Condition
In brief
The objective of this study is to determine the performance of the ID NOW™ CT/NG test in male urine, female urine, and self-collected vaginal swabs when tested by intended users (i.e., untrained operators). ID NOW™ CT/NG test results will be compared to results from up to three (3) FDA cleared CT/NG nucleic acid amplification tests (NAATs) for each sample type.
Key facts
- Study ID
- NCT06395675
- Run by
- Abbott Rapid Dx
- People needed
- 7100
- Starts
- 2024-07-09
- Expected to finish
- 2025-01-09
- Last updated by the study team
- 2024-05-02
Who can join
Age: 14 and older. Sex: any. Healthy volunteers: accepted.
Where it is running
- LSU Crescent Care Sexual Health Clinic — New Orleans, Louisiana, United States
Full record on ClinicalTrials.gov
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