Test Price
850 AED✅ Home Collection Available
Male Hypogonadism Panel in UAE | 850 AED | PDPL Compliant
Executive Summary & Core Metrics
Clinical Utility
Multi-analyte endocrine assessment for diagnosing primary and secondary hypogonadism, guiding testosterone therapy, and evaluating fertility potential.
Accuracy
99.9% diagnostic sensitivity via ISO 15189 accredited CLIA and LC-MS/MS gold-standard methodologies.
Logistics
VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection available daily from 8 AM to 11 PM.
Price
850 AED — includes physician-guided result interpretation and direct billing support.
Test Overview & Methodology
The Hypogonadism Panel (Male) is a targeted multi-analyte endocrine assessment measuring total and free testosterone, sex hormone-binding globulin (SHBG), luteinizing hormone (LH), follicle-stimulating hormone (FSH), and estradiol. This panel differentiates primary, secondary, and mixed hypogonadism, guides testosterone therapy, and supports anti-aging and sports optimization protocols. All assays are performed via CLIA and definitive LC–MS/MS, ensuring diagnostic accuracy compliant with Federal Decree-Law No. 4 of 2016 on Medical Liability.
| Feature | Our Hypogonadism Panel (UAE) | Standard Total Testosterone |
|---|---|---|
| Precision | 99.9% Sensitivity via ISO‑validated LC‑MS/MS | CLIA only; variable accuracy ±15% |
| Methodology | CLIA + LC‑MS/MS (gold standard) | CLIA alone |
| Turnaround Time | 3 business days | 5–7 days |
| Clinical Scope | Full pituitary–testicular axis (T, free T, SHBG, LH, FSH, E2) | Total testosterone only |
Physician Insight & Safety Protocols
“Low testosterone can significantly impact vitality, mood, and metabolic health. This panel provides a comprehensive view of pituitary–testicular function, but results must always be interpreted alongside clinical history, physical examination, and lifestyle factors. Never discontinue or adjust prescribed hormone therapy without direct medical supervision.”
— Dr. Ajay Singh, General Practitioner, DHA License 36234132
Advisory on Pre-Test Preparation
To ensure accurate baseline measurements, patients must fast for 8–12 hours, provide a morning sample (between 7:00 AM and 10:00 AM), and avoid strenuous exercise, alcohol, and sexual activity for 24 hours prior to collection. Certain supplements including DHEA, androstenedione, and selective estrogen receptor modulators must be stopped 6 weeks before testing. Patients with acute febrile illness or severe liver/renal impairment should defer testing until resolution.
Exclusion Criteria & Emergency Red Flags
- Exclusions: Recent intramuscular testosterone injection (within 6 weeks), current use of DHEA, androstenedione, selective estrogen receptor modulators, or severe liver/renal impairment.
- Red Flags – Seek Immediate Medical Attention: Sudden severe headache with visual disturbances, testicular torsion symptoms, chest pain, or signs of anaphylaxis after blood draw.
Patient FAQ & Clinical Guidance
1. What is the Hypogonadism Panel (Male) used for?
This panel is designed to diagnose primary and secondary hypogonadism, assess fertility potential, and monitor testosterone replacement therapy effectiveness. It offers a comprehensive view of the pituitary–testicular axis beyond standard total testosterone alone.
2. How should I prepare for the blood draw?
You must fast for 8-12 hours, provide a morning sample, and avoid strenuous exercise, alcohol, and sexual activity 24 hours prior. Certain supplements must be stopped 6 weeks before testing. Please consult with your physician for complete preparation instructions.
3. How quickly will I receive my results?
Results are reported within 3 business days from sample receipt. Samples received on Monday or Thursday before 9:00 AM will be processed in the next available batch. A telephonic clinical guidance session is included for result interpretation.
UAE Regulatory & Data Privacy Adherence
Data Privacy & Security: DNA Labs UAE operates in full compliance with Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields. All patient data is encrypted, stored in UAE-based servers, and never shared without explicit consent.
Clinical Safety: All diagnostic procedures adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability, ensuring patient consent, clinical governance, and laboratory standards are met at every stage.
Clinical & Logistical Metadata
| Test Name | Hypogonadism Panel (Male) – Total Testosterone, Free Testosterone, SHBG, LH, FSH, Estradiol |
| Price (AED) | 850 AED |
| Turnaround Time | 3 business days from sample receipt |
| Sample Type / Matrix | Peripheral venous blood (serum) – VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (available daily 8 AM–11 PM) |
| Methodology Used | CLIA + LC-MS/MS (gold standard) |
| ICD-10-CM Code | E29.1 (Testicular hypofunction) |
| LOINC Code | 2986-8 (Testosterone [Mass/volume] in Serum or Plasma) |
| DHA Facility & Address | DHA License 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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