DIAGNOSTICA IVD
DIAGNOSTICA IVD

Sexually Transmitted Infection (STI) Test 4-Panel Urogynaecological

€99,00

Sample required: Colli-Pee® device (male/female) or Vaginal Swab (female only) 

Storage: Stable at room temperature (Colli-Pee® 30 days; Swab 90 days) 

Methodology: Real-Time PCR with fluorescent probes (CE-IVD marked) 

Turnaround time: 3–5 weeks 

The IVD Diagnostic Test for STIs — Urogynecological Panel  is a molecular analysis using Real-Time PCR specifically for the detection of genitourinary mycoplasmas and ureaplasmas (Ureaplasma urealyticum, Ureaplasma parvum, Mycoplasma hominis, Trichomonas vaginalis). Can be performed at home via Colli-Pee® or vaginal swab, it is the ideal diagnostic tool for in-depth analysis in the presence of persistent symptoms, recurrent infections, or couple fertility issues when standard urine cultures and swabs are negative. 

Test method

Informed consent

artt. 13 e 9 Reg. UE 2016/679 - GDPR

Required

Consent to the processing of health-related data for care purposes (section 3.a).

Required

Consent to receiving the service via teleconsultation, with the limits described in the notice.

Optional

Consent to possible recording of the session (not required for the service).

How does it work?

  • Self-collection: Perform the collection at home in complete privacy. 
  • Sample shipment: Send the test tube using the provided prepaid envelope, with no need for a cold chain. 
  • Analysis and report: The laboratory uses Real-Time PCR technology. The official IVD report will be available online within 3–5 weeks. 

Why choose?

  • Recommended when the clinical picture, symptoms, and medical history point toward a specific group of microorganisms. This solution is ideal for those who already have a precise indication or medical prescription.
  • Diagnosis of challenging microorganisms: Mycoplasmas and ureaplasmas are difficult to detect with classic cultures; Real-Time PCR eliminates the risk of false negatives.
  • Resolution of chronic conditions: Essential when symptoms persist but standard tests are consistently negative.
  • Maximum privacy: Procedure can be performed entirely within the home.

Who is it for?

  • Those presenting with persistent or recurrent urogynecological symptoms (pelvic discomfort, urethral burning, recurrent vaginitis). 
  • Couples undergoing fertility treatment or Medically Assisted Procreation (MAP). 
  • Individuals with suspected Pelvic Inflammatory Disease (PID) or chronic prostatitis that is abacterial in traditional cultures.

Disclaimer

  • IVD Diagnostic Value: The report constitutes an official CE-IVD diagnostic aid for the specialist physician. 
  • Clinical Management: Any positive result requires contextualization by a physician to initiate targeted therapy and, if necessary, treat the partner. 
  • Contraindications for sampling: For women, do not perform the swab during menstruation or while undergoing topical ovular therapies. 


The information provided is for purely informational purposes and does not replace the advice, diagnosis, or consultation of a specialist physician.