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Medical information Clinical review pending

Infection Testing

Trichomonas Vaginalis RNA Detection Qualitative Test

Detects the presence of Trichomonas vaginalis RNA to diagnose Trichomoniasis, a common sexually transmitted infection, using Real Time PCR technology.

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
Confirm with the laboratory before booking. Typically requires a vaginal swab or urine sample.
Results
Results are typically available within 36 hours via phone and 48 hours via email. Confirm with the laboratory before booking.
Preparation
Confirm with the laboratory before booking. May involve specific instructions regarding recent sexual activity or medication use.
Test priceKSh 11,900

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 Trichomonas Vaginalis 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 of Trichomoniasis (e.g., unusual discharge, itching, irritation).
  • ✓Individuals with multiple sexual partners.
  • ✓Individuals diagnosed with other sexually transmitted infections.
  • ✓Pregnant women.
  • ✓Individuals with recent unprotected sexual contact with a potentially infected partner.
02

In plain language

What this test helps you understand

This test aids in the accurate diagnosis of Trichomoniasis, allowing for timely and appropriate treatment to prevent complications and reduce transmission.
The Trichomonas Vaginalis RNA Detection Qualitative Test is a diagnostic tool used to identify the Trichomonas vaginalis parasite, which causes the sexually transmitted infection Trichomoniasis. This test uses advanced Real Time PCR technology to detect the parasite's RNA in a sample. Early detection is important for prompt treatment, reducing the risk of complications and transmission. This test specifically measures the RNA of the Trichomonas vaginalis organism. Results are typically available within 48 hours via email and 36 hours via phone. A positive result indicates the presence of the parasite, while a negative result suggests no infection. Discuss your results with a healthcare provider for appropriate 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 →
PreparationConfirm with the laboratory before booking. May involve specific instructions regarding recent sexual activity or medication use.
SampleConfirm with the laboratory before booking. Typically requires a vaginal swab or urine sample.
MethodologyReal Time PCR (Polymerase Chain Reaction) technology is used to detect the RNA of the Trichomonas vaginalis organism.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test detects the presence of Trichomonas vaginalis RNA. A negative result does not completely rule out infection, especially if the sample was collected long after exposure or if the parasite load is very low. Consult a healthcare provider 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

Trichomoniasis is a common sexually transmitted infection caused by the parasite Trichomonas vaginalis.
The Real Time PCR method used is highly accurate for detecting the presence of Trichomonas vaginalis RNA.
A vaginal swab or urine sample is typically required. Please confirm specific requirements with the laboratory.
Results are generally available within 36 hours via phone and 48 hours via email. Confirm with the laboratory before booking.
If you test positive, consult your healthcare provider immediately to discuss treatment options.
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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