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Medical information Clinical review pending

Infection Testing

N Gonorrhoea RNA Detection Qualitative Test

Detects the presence of Neisseria gonorrhoeae, the bacteria causing gonorrhoea, using Real Time PCR technology. This test is important for diagnosing this common STI and preventing complications.

General information only: This page is not a diagnosis or personal medical advice. A qualified clinician should decide whether testing is appropriate and interpret results in context.

Review status: No completed medical review is recorded for this page.

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Counselor guidance included Confidential handling Kenya-wide coordination

At a glance

Plan your test

Sample
Urethral or vaginal swab, cervical discharge, rectal swab, urine, or blood sample.
Results
Results typically available within 36 hours via phone or 48 hours via email. Confirm with the laboratory before booking.
Preparation
Confirm with the laboratory before booking. Patients are required to sign a consent document and provide relevant clinical history.
Test priceKSh 11,560

Payment: M-Pesa and card options can be confirmed during booking.

Insurance & government schemes

Is this test covered for you?

We help you verify whether the N Gonorrhoea RNA Detection Qualitative Test test can be claimed against your insurer, employer scheme or a Kenyan government health scheme — before you book. Coverage depends on your plan, clinical indication and your provider's rules; final approval always rests with them.

Talk to a claims advisor

Providers & schemes we can help you check

Government & public schemes

SHIF — Social Health Insurance Fund Linda Mama EduAfya NHIF (legacy cards)

Eligibility and benefits follow the current rules of the Social Health Authority (SHA) and applicable government programmes.

Private insurers & employer schemes

Jubilee Health AAR APA Britam CIC Madison Resolution Pioneer Minet Old Mutual GA Life Heritage + other licensed insurers

Names shown for identification only — listing does not imply partnership or guarantee of coverage.

Have these ready when we check

  • Insurer or scheme name & policy / member number
  • A clinician's request / prescription for the test
  • Pre-authorisation letter, if your plan requires one

Free coverage check

Ask us to verify your cover

Send your details and our claims team confirms what documents you need and whether pre-authorisation applies — usually the same working day.

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Used only to process your coverage check — see our Privacy Policy. Verification support is free and does not guarantee your provider will pay.

01

Start with fit

Is this the right test for you?

The best test starts with a clear clinical question. These are common reasons a clinician or family may consider this test.

  • ✓Symptoms suggestive of gonorrhoea (e.g., discharge, painful urination)
  • ✓History of sexually transmitted infections
  • ✓Unprotected sexual activity
  • ✓Partner diagnosed with gonorrhoea
  • ✓Screening in pregnant women
  • ✓Confirmation of suspected infection
02

In plain language

What this test helps you understand

This test is used to detect the presence of Neisseria gonorrhoeae RNA, aiding in the diagnosis of gonorrhoea infection.
The N Gonorrhoea RNA Detection Qualitative Test is a diagnostic tool used to identify Neisseria gonorrhoeae, the bacterium responsible for gonorrhoea, a common sexually transmitted infection (STI). Early detection is crucial as untreated gonorrhoea can lead to serious health issues. This test uses advanced Real Time PCR technology for accurate and reliable results, enabling timely treatment.

This test specifically looks for the genetic material (RNA) of Neisseria gonorrhoeae in samples such as urethral or vaginal swabs, cervical discharge, rectal swabs, urine, or blood.

Consider this test if you are experiencing symptoms like unusual discharge, pain during urination, or pelvic pain. It is also recommended for individuals with a history of STIs, those engaging in unprotected sex, partners of individuals diagnosed with gonorrhoea, and pregnant women.

Getting tested provides an accurate diagnosis, allows for prompt treatment, helps prevent complications like infertility, and offers peace of mind. Our services are confidential and professional.

Results will indicate whether the Neisseria gonorrhoeae bacterium was detected in your sample. A positive result confirms the infection, while a negative result suggests no infection was found. Discuss your results with a healthcare provider for appropriate follow-up.
03

Medical review status

Clinical review pending

A completed medical review is not recorded for this page. No clinician has endorsed the information shown here. Please discuss testing decisions with a qualified healthcare professional.

Meet the DNA Labs Kenya medical team →
04

A simple process

What happens next?

You do not have to navigate the test alone. We help you move from question to next step.

1

Speak with us

We check the test and answer your questions before collection.

2

Give your sample

Choose home collection or a coordinated hub visit in Kenya. We explain whether this test uses a cheek swab or blood draw.

3

Understand your report

A counselor helps you understand the result and the next steps.

05

Choose your collection

Home collection or a lab visit

We will explain the sample, preparation, and next steps before anything is collected.

Home collection

Choose a coordinated visit at home or another convenient location. Our team confirms the appointment and sample requirements in advance.

Lab or hub visit

Prefer to visit a coordinated location? We can guide you to the right hub and explain what to expect when you arrive.

Ask about locations →
PreparationConfirm with the laboratory before booking. Patients are required to sign a consent document and provide relevant clinical history.
SampleUrethral or vaginal swab, cervical discharge, rectal swab, urine, or blood sample.
MethodologyReal Time PCR (Polymerase Chain Reaction)
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test detects the presence of Neisseria gonorrhoeae RNA. It does not differentiate between active and past infection. Confirm with the laboratory before booking.
06

Read your report

What common result terms mean

PositiveA finding was identified. Your clinician or counselor will explain what it means for your care.
NegativeThe specific finding tested for was not identified. It does not rule out every possible cause.
VUSA variant was found, but current evidence is not enough to classify it. Your counselor can explain follow-up.
07

Questions people ask

Frequently asked questions

Gonorrhoea is a common sexually transmitted infection (STI) caused by the bacterium Neisseria gonorrhoeae. It can affect the genitals, rectum, and throat.
The N Gonorrhoea RNA Detection Qualitative Test using Real Time PCR is highly accurate in detecting the presence of the bacteria.
If your result is positive, it means the bacteria was detected. You should consult a healthcare provider immediately to discuss treatment options.
Yes, all testing and results are handled with strict confidentiality.
Confirm with the laboratory before booking regarding insurance coverage.
08

Collaboration

Open for partnership with hospitals, clinics, doctors & researchers

Whether you are referring patients, building a research programme or supporting students, we work as an extension of your team — with responsive communication and clear scientific standards.

Hospitals & clinics

Referral pathways, coordinated sample logistics and shared reporting that fits your clinical workflow.

Doctors & specialists

LOINC-coded reports, ACMG-based variant classification and a direct scientific line for complex cases.

Research institutions

Sanger sequencing, NGS panels and custom assays — with project design support, batch pricing and agreed turnaround commitments.

Students & academic projects

Discounted laboratory services for college, master's and PhD research projects — including proposal guidance and cost-effective batch testing.

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09

Trust & transparency

Sources, standards & how this page is maintained

Standards & references

  • ACMG/AMP technical standards for sequence variant interpretation
  • ClinGen curation and gene–disease validity frameworks where applicable
  • LOINC-coded reporting for interoperable results
  • ISO 9001:2015 quality management; ISO 15189 accreditation in progress

Page provenance

  • Last updated: September 27, 2026
  • Medical review: not yet completed
  • Written for patients & clinicians in Kenya; reviewed periodically against current guidance

Medical disclaimer: this page is general information, not a diagnosis or personal medical advice. Testing decisions and result interpretation should be made with a qualified healthcare professional.

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