Royal Oak, MONCT06815536Now EnrollingIRB Ready

Neisseria Gonorrheae Infection Clinical Trial in Royal Oak, MO

Access cutting-edge neisseria gonorrheae infection treatment through this clinical trial at a research site in Royal Oak. Study-provided care at no cost to qualified participants.

Sponsored by Duke University

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Expert Care in Royal Oak

Access neisseria gonorrheae infection specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related neisseria gonorrheae infection treatment provided free

Apply for This Royal Oak Location

Check if you qualify for this neisseria gonorrheae infection clinical trial in Royal Oak, MO

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Why Participate?

  • No-Cost Study Care

  • Local to Royal Oak

    Convenient for MO residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Royal Oak site if eligible
  4. 4Begin participation

About This Neisseria Gonorrheae Infection Study in Royal Oak

The goal of this study is to learn if a few investigational tests can correctly find the gene mutation (mutant allele gyrA 91F) that predicts ciprofloxacin resistance in clinical specimens that harbor Neisseria gonorrhoeae. The main question the study aims to answer: Can the investigational reflex test find the correct gene mutation (Neisseria gonorrhoeae gyrA 91F or gyrA 91S) as compared to the sequenced result? Specimens that are collected for routine clinical care and harbor Neisseria gonorrhoeae will be evaluated in this study.

Sponsor: Duke University

Who Can Participate

Inclusion Criteria

Be N. gonorrhoeae-positive on an FDA-cleared molecular assay
Have sufficient N. gonorrhoeae-positive specimen volume for testing using the corresponding investigational reflex test and genetic sequencing
Undergo proper handling and storage conditions

Exclusion Criteria

The N. gonorrhoeae-positive specimen media is not compatible with the investigational reflex test(s) at the laboratory site
The N. gonorrhoeae-positive specimen is not clearly labeled by the laboratory to link to basic epidemiologic data (age, sex) and source

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Royal Oak?

Yes, this clinical trial (NCT06815536) has an active research site in Royal Oak, MO that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Neisseria Gonorrheae Infection Treatment Options in Royal Oak, MO

If you're searching for neisseria gonorrheae infection treatment options in Royal Oak, MO, this clinical trial (NCT06815536) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Royal Oak research site is actively enrolling participants for this clinical trial. You'll receive care from experienced neisseria gonorrheae infection specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

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Take the first step toward participating in this groundbreaking clinical trial

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