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NCT05286931 · ClinicalTrials.gov registry record · NA
SpeeDx Ciprofloxacin gyrA Assay for N. Gonorrhoeae Gonococcal Infection
A NA study of Neisseria Gonorrhoeae Infection, sponsored by University of Washington.
- Recruiting
- Registry status
- NA
- Development phase
- 1,800
- Enrollment target
- 1
- Study location
NCT05286931: Recruiting NA study of Neisseria Gonorrhoeae Infection, sponsored by University of Washington.
NCT05286931 is a NA study of Neisseria Gonorrhoeae Infection that is actively recruiting participants, run by University of Washington. The registered enrollment target is 1,800 participants, above the 1,139-participant average among 3 other Neisseria Gonorrhoeae Infection trials with a reported enrollment target (58% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05286931, a NA study of Neisseria Gonorrhoeae Infection, is actively recruiting participants, sponsored by University of Washington.
- RECRUITING
- Registry status
- NA
- Development phase
- 1,800 participants
- Enrollment target
- 1
- Study location
Study Summary
This study aims to test the effectiveness of using of SpeeDx Resistance Plus assay to guide treatment of Neisseria gonorrhoeae (Ng) in a sexual health clinic setting.
Primary Outcome
Number and proportion of patients who test positive for Neisseria Gonorrhea (NG) and are gyrA wildtype of all patients enrolled/screened for NG
Conditions Studied
Interventions
- DRUG Ciprofloxacin 500 mg
Study Locations (1)
Washington
- Public Health -- Seattle & King County Sexual Health Clinic - Seattle
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,800 participants |
| Start Date | 2022-03-03 |
| Est. Completion | 2026-12-31 |
| Phase | NA |
What NCT05286931 shows while recruiting
NCT05286931 is an interventional study that assigns participants to a tested intervention. Its 1,800 participants enrollment target places it among the larger protocols in the corpus, above the 1,139-participant average among 3 other Neisseria Gonorrhoeae Infection trials with a reported enrollment target (58% higher).
The record links to 1 condition, with Neisseria Gonorrhoeae Infection appearing as the primary indexed condition, and to 1 intervention - of which Ciprofloxacin 500 mg is the first listed.
NCT05286931 reports a single indexed study location in Washington.
Frequently Asked Questions
What is clinical trial NCT05286931 about?
NCT05286931 is a clinical study titled "SpeeDx Ciprofloxacin gyrA Assay for N. Gonorrhoeae Gonococcal Infection". This study aims to test the effectiveness of using of SpeeDx Resistance Plus assay to guide treatment of Neisseria gonorrhoeae (Ng) in a sexual health clinic setting.
What is the current status of trial NCT05286931?
This trial is currently recruiting. It is a NA study. The enrollment target is 1,800 participants. The study started on 2022-03-03. Estimated completion is 2026-12-31.
What conditions does trial NCT05286931 study?
This clinical trial studies the following conditions: Neisseria Gonorrhoeae Infection.
What interventions are being tested in trial NCT05286931?
The interventions under investigation include: Ciprofloxacin 500 mg (DRUG).
Who is sponsoring clinical trial NCT05286931?
This trial is sponsored by University of Washington, which has 1,048 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05286931 being conducted?
This trial has 1 study location across Washington. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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