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Medical information Clinical review pending

Infection Testing

Trichomonas Vaginalis Bacterial Load Test

Detects the presence and load of Trichomonas vaginalis, a common sexually transmitted infection, using Real Time PCR for accurate diagnosis.

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
Vaginal swab. Confirm specific collection requirements with the laboratory before booking.
Results
Results are typically available via email within 48 hours and by phone within 36 hours. Confirm exact turnaround time with the laboratory before booking.
Preparation
No specific preparation is required for this test. However, please inform the laboratory if you are currently taking any medications or have any relevant medical history.
Test priceKSh 17,000

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 Trichomonas Vaginalis Bacterial Load 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 vaginal discharge, itching, discomfort)
  • ✓History of STIs
  • ✓Multiple sexual partners
  • ✓Partner diagnosed with Trichomonas vaginalis
  • ✓Routine screening for sexually active individuals
  • ✓Pregnant women
02

In plain language

What this test helps you understand

This test helps diagnose Trichomonas vaginalis infection, assess the infection load, guide treatment decisions, and monitor treatment effectiveness. It is crucial for managing STIs and preventing transmission.
The Trichomonas Vaginalis Bacterial Load Test is a diagnostic procedure used to identify the presence of the Trichomonas vaginalis parasite, a common cause of sexually transmitted infections (STIs). This test is important for individuals experiencing symptoms or those at risk, as early detection allows for effective treatment and helps prevent complications. This test specifically measures the load of Trichomonas vaginalis in the body, providing information about the infection's severity. It uses the Real Time PCR method, known for its accuracy in identifying the parasite's genetic material. Taking this test allows for accurate identification, timely treatment, and prevention of transmission to partners. Discuss your results with a healthcare provider to understand the implications and 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 →
PreparationNo specific preparation is required for this test. However, please inform the laboratory if you are currently taking any medications or have any relevant medical history.
SampleVaginal swab. Confirm specific collection requirements with the laboratory before booking.
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 Trichomonas vaginalis DNA. It does not differentiate between live and dead organisms. False negatives can occur if the sample is inadequate or if the parasite load is very low. 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

Trichomonas vaginalis is a microscopic parasite that causes a common sexually transmitted infection (STI), often referred to as 'trichomoniasis'.
Early detection of Trichomonas vaginalis allows for prompt treatment, preventing potential complications and reducing the risk of transmission to sexual partners.
A sample is typically collected using a vaginal swab. Specific instructions will be provided by the laboratory or healthcare provider.
The Real Time PCR method used for this test is highly accurate in detecting the genetic material of Trichomonas vaginalis.
It is important to discuss your results with a healthcare provider. They can interpret the findings in the context of your health history and recommend appropriate treatment if necessary.
The sample collection process using a vaginal swab may cause mild discomfort but is generally not painful.
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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