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Diagnostic options ยท UAE

STI PCR tests in Dubai & UAE

Compare available STI PCR tests, their listed prices and the information provided for each option. Test selection and preparation should be discussed with your clinician.

Tests in this category

2

Listed price range

650.00โ€“800.00 AED

Clinical preparation

Confirm test-specific instructions with your clinician or laboratory.

Compare available tests

STI PCR test prices

Showing 1โ€“2 of 2 matching tests.

STI PCR diagnostic tests, details, and listed prices
Test and description Specimen Typical duration Price Options
TEST-599
Chlamydia trachomatis and Neisseria gonorrhoeae PCR Qualitative Test

This diagnostic test evaluates the presence of genetic material from Chlamydia trachomatis and Neisseria gonorrhoeae bacteria in a patient sample.

Urine (first-void) or urogenital swab (urethral, cervical, vaginal) Next-day report (24 hours from sample receipt) 800.00 AED
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View test specifications and preparation
What it measures
["Chlamydia trachomatis DNA", "Neisseria gonorrhoeae DNA", "Antimicrobial resistance profile (optional)"]
Parameters
[{"name": "Chlamydia trachomatis DNA", "reference_range": "Not Detected"}, {"name": "Neisseria gonorrhoeae DNA", "reference_range": "Not Detected"}, {"name": "Antimicrobial Resistance Profile", "reference_range": "Susceptible / Resistant (if WGS performed)"}]
Preparation
["Avoid urinating for at least 1 hour before providing a first-void urine sample.", "Inform your doctor of all current medications, especially antibiotics.", "Do not discontinue prescribed medication without consulting your physician."]
Indications
["Screening for sexually transmitted infections", "Diagnosis of symptomatic infections", "Partner notification follow-up", "Evaluation of treatment failure"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 43304-6 ICD-10: A56.0, A54.0
Clinical summary
This diagnostic test evaluates the presence of genetic material from Chlamydia trachomatis and Neisseria gonorrhoeae bacteria in a patient sample.
TEST-2630
Neisseria gonorrhoeae Qualitative PCR Test

This test detects the presence or absence of Neisseria gonorrhoeae DNA in a patient sample.

Urine or Genital Swab (Urethral/Endocervical) Next-day report (samples received by 11 AM) 650.00 AED
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View test specifications and preparation
What it measures
["Neisseria gonorrhoeae DNA", "Opal gene (multicopy)"]
Parameters
[]
Preparation
["Provide a first-morning urine sample", "Avoid urinating for at least 1 hour before collection", "Avoid douching or using vaginal creams for 24 hours prior (for swabs)"]
Indications
["Symptomatic diagnosis", "Asymptomatic screening in at-risk populations", "Test-of-cure following treatment"]
Measurement technique
Confirm with laboratory
Codes
LOINC: 50387-0 ICD-10: A54.9, Z11.3, A54.00
Clinical summary
This test detects the presence or absence of Neisseria gonorrhoeae DNA in a patient sample.

Category overview

STI PCR: overview

Persistent concerns regarding intimate infections require exact answers, and advanced molecular detection offers the essential clarity needed for targeted, effective relief. Operating within our Molecular Diagnostics division, our STI PCR testing uses highly sensitive genomic techniques to quickly identify the DNA or RNA of various sexually transmitted pathogens. Instead of acting as a final standalone diagnosis, this deeply precise molecular data equips your infectious disease specialist or primary physician with the crucial insights required for customized, proactive medical guidance. Renowned across top diagnostic labs in the UAE, DNA Labs UAE promises absolute patient privacy coupled with exceptionally fast, meticulous results. Empower your health journey: explore our STI PCR testing in the UAE below to book a highly confidential test, arrange a safe home sample collection, or consult our specialized medical team.

Before booking

Use the test details as a conversation starter

The right diagnostic option depends on your reason for testing and individual circumstances. Check the listed specimen and timing, then confirm any preparation requirements with the ordering clinician or laboratory before collection.