Trichomonas vaginalis RNA Qualitative Test in Dubai | 700 AED | DHA Licensed

Executive Summary & Core Metrics

Accuracy Guarantee

99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139).

Premium Logistics

VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Available daily from 8 AM to 11 PM).

Clinical Guidance

Post-Test Telephonic Consultation for result interpretation by a DHA-licensed General Practitioner.

Insurance & Billing

Direct Billing Verification via WhatsApp: +971 54 548 8731

Test Overview & Methodology

The Trichomonas vaginalis RNA Qualitative Test uses real-time PCR (qPCR) to directly detect active infection with unparalleled accuracy, confirming the presence of the parasite even in low-load samples. This eliminates the high false-negative rate associated with traditional microscopy and culture methods.

Parameter	Our Test: T. vaginalis RNA qPCR	Closest Alternative: Wet Mount / Culture
Diagnostic Sensitivity	>99%	60–80%
Methodology	Real‑time PCR (qPCR) – RNA target	Microscopy or culture (slower, less sensitive)
Turnaround Time	36–48 hours (phone/email)	3–7 days
Sample Types	Vaginal swab, urethral swab, urine (first‑void), cervical discharge	Vaginal swab / urethral swab (requires viable organisms)
Regulatory Approval	DHA Licensed, ISO 9001:2015	Variable

Physician Insight & Safety Protocols

Dr. Ajay Singh (DHA License: 36234132) – “The Trichomonas vaginalis RNA qualitative test is a highly reliable method for confirming active infection. However, a negative result does not rule out other sexually transmitted infections, and a positive result must always be accompanied by partner notification and appropriate treatment. Do not alter any prescribed medication without first consulting your healthcare provider.”

🚨 Patient Safety – Exclusion Criteria & Red Flags

Recent antibiotic/antifungal therapy (within 2 weeks) – may temporarily suppress RNA
Vaginal douching or use of intravaginal products 24‑48 hours prior to sampling
Active menstruation – reschedule sample collection to mid‑cycle (if possible)
Emergency Red Flags: Sudden severe pelvic pain, high fever, abnormal vaginal bleeding, signs of ectopic pregnancy – seek immediate ER care

Patient FAQ & Clinical Guidance

1. What exactly does the Trichomonas vaginalis RNA Qualitative Test detect?

This test directly identifies genetic material (RNA) of active Trichomonas vaginalis parasites with extremely high accuracy. Unlike older methods, it confirms an ongoing infection even when parasites are scarce, enabling prompt targeted antibiotic treatment and reducing transmission risk.

2. How is the sample collected and is the procedure painful?

A simple sample of vaginal discharge, a urethral swab, or a first-void urine specimen is collected by a trained nurse. The process is quick and minimally uncomfortable. Specimens are placed in a transport medium and delivered to the lab via a certified cold chain to ensure result accuracy.

3. What does a positive result mean and what should I do next?

A positive RNA result confirms an active Trichomonas vaginalis infection that typically requires a single-dose antibiotic treatment. You should immediately consult your physician, inform any recent sexual partners, and avoid sexual contact until both partners have completed treatment and follow-up testing. Telephonic guidance from our DHA-licensed doctor will explain the next steps.

UAE Regulatory & Data Privacy Adherence

Data Protection & Clinical Safety Compliance:

All personal health data is processed in accordance with Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL).
Use of information and communication technology in health fields adheres to Federal Law No. 2 of 2019.
Patient consent and clinical safety protocols follow Federal Decree-Law No. 4 of 2016 on Medical Liability.
Laboratory accreditation: ISO 9001:2015 (Cert: INT/EGQ/2509DA/3139).

Clinical & Logistical Metadata

Test Name	Trichomonas vaginalis RNA Qualitative Test
Price (AED)	700
Turnaround Time	36–48 hours
Sample Type / Matrix	Vaginal swab, urethral swab, first-void urine, cervical discharge
Methodology Used	Real-time PCR (qPCR) targeting T. vaginalis RNA
ICD-10-CM Code	A59.00, A59.01, A59.9
LOINC Code	97911-7
DHA Facility License & Address	License: 1143 \| Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE

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