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Medical information Clinical review pending

Genetic Testing

Chlamydia Trachomatis and Neisseria Gonorrhoeae PCR Qualitative Test

Detects Chlamydia Trachomatis and Neisseria Gonorrhoeae, common STIs, using a sensitive PCR test. Early detection is key for timely treatment and preventing complications. Confirm price and availability before booking.

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
First morning urine (15 ml minimum) in a sterile container, or a vaginal, endocervical, or conjunctival swab in normal saline.
Results
Results are typically available the next day. Confirm exact turnaround time with the laboratory before booking.
Preparation
Collect the first morning urine sample for best results. Avoid urinating for at least one hour before collection. If providing a swab, follow specific instructions from your healthcare provider or the laboratory.
Test priceKSh 13,000

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 Chlamydia Trachomatis and Neisseria Gonorrhoeae PCR 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 of STI (e.g., unusual discharge, painful urination)
  • ✓Multiple sexual partners
  • ✓Inconsistent use of barrier protection
  • ✓Known exposure to an STI
  • ✓Routine screening for sexually active individuals
  • ✓Partner diagnosed with an STI
02

In plain language

What this test helps you understand

This test is used to detect the presence of Chlamydia Trachomatis and Neisseria Gonorrhoeae DNA in a patient sample, aiding in the diagnosis of these common sexually transmitted infections.
This test helps identify Chlamydia Trachomatis and Neisseria Gonorrhoeae, two common sexually transmitted infections (STIs). Early diagnosis is important because untreated STIs can lead to serious health issues. This test uses Real Time PCR technology for accurate detection. It is recommended for individuals experiencing symptoms, those with risk factors, or anyone concerned about potential exposure. Getting tested provides peace of mind and allows for prompt treatment if needed. Results are typically available the next day. Discuss your results with your healthcare provider to understand the next steps.
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 →
PreparationCollect the first morning urine sample for best results. Avoid urinating for at least one hour before collection. If providing a swab, follow specific instructions from your healthcare provider or the laboratory.
SampleFirst morning urine (15 ml minimum) in a sterile container, or a vaginal, endocervical, or conjunctival swab in normal saline.
MethodologyReal Time Polymerase Chain Reaction (PCR) - Qualitative detection.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test detects the presence of the organisms' DNA but does not differentiate between active and past infections. A negative result does not completely rule out an infection, especially if exposure was recent. Consult your doctor for interpretation.
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

This test detects the genetic material of Chlamydia Trachomatis and Neisseria Gonorrhoeae, the bacteria that cause Chlamydia and Gonorrhoea infections.
Early detection allows for prompt treatment, which can prevent serious long-term health complications, including infertility and pelvic inflammatory disease.
The preferred sample is a first morning urine sample. Swabs from the vagina, cervix, or conjunctiva can also be used. Confirm requirements with the lab.
The Real Time PCR method used is highly sensitive and specific for detecting these infections.
If you receive a positive result, it's important to consult with your healthcare provider immediately to discuss treatment options.
Yes, patient confidentiality is maintained according to ethical and legal standards. Discuss any specific privacy concerns with the laboratory.
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.

Explore partnerships
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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