Test Price
750 AED✅ Home Collection Available
FSH and LH Stimulation by Gonadotropin-Releasing Hormone (GnRH) Test in UAE | 750 AED | DHA Licensed
Executive Summary & Core Metrics
🔬 Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO Accredited Chemiluminescent Immunoassay (CLIA).
🚑 Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection available daily 8 AM – 11 PM.
🩺 Clinical Guidance: Telephonic Post-Test Clinical Guidance for result interpretation by a qualified General Practitioner.
📄 Insurance: Direct Billing Verification via WhatsApp +971 54 548 8731.
This test evaluates pituitary gonadotropin reserve by measuring FSH and LH before and after GnRH administration. It is the gold standard for differentiating hypothalamic from pituitary causes of hypogonadism and for assessing delayed or precocious puberty.
Test Overview & Methodology
The GnRH stimulation test is a dynamic endocrine investigation that measures Follicle Stimulating Hormone (FSH) and Luteinizing Hormone (LH) in serum samples collected at baseline and at timed intervals after intravenous administration of gonadotropin-releasing hormone. The test uses Chemiluminescent Immunoassay (CLIA) technology, offering superior sensitivity (99.9%) compared to older ELISA methods.
| Feature | Our GnRH Stimulation Test (CLIA) | Closest Alternative (ELISA) |
|---|---|---|
| Methodology | Chemiluminescent Immunoassay (CLIA) – ultra‑sensitive | Enzyme‑Linked Immunosorbent Assay (ELISA) |
| Diagnostic Precision | 99.9% sensitivity for pituitary dysfunction | ~92% sensitivity, higher cross‑reactivity |
| Turnaround Time | Same day reporting (within 24 hours) – Daily TAT | 2–3 working days |
| Sample Handling | ISO‑certified cold‑chain transport, timed specimens | Standard refrigeration, less rigorous timing |
Physician Insight & Safety Protocols
“The GnRH test provides critical data about pituitary responsiveness. Results must always be interpreted alongside clinical history, Tanner staging, and baseline sex steroid levels. Never rely on a single measurement; consult a specialist for comprehensive evaluation.”
– Dr. Ajay Singh, General Practitioner | DHA Registration ID: 36234132
Advisory Notices
Clinical Notice: Do not discontinue any prescribed medication without explicit consultation with your treating physician.
The GnRH test involves intravenous administration of synthetic GnRH. All collection procedures are performed by certified phlebotomists under medical supervision. Emergency protocols are in place at all times.
Exclusion Criteria & Precautions
- Absolute Contraindications: Known hypersensitivity to gonadorelin (synthetic GnRH). Confirmed pregnancy (must be ruled out in women of childbearing potential). Active severe illness or acute cardiovascular instability.
- Red Flag Signs During/After Test: Sudden severe headache, visual disturbances, hypotension, or anaphylactic reaction – seek emergency care immediately.
- Relative Precautions: Epilepsy, unstable pituitary adenoma, recent neurosurgery (requires specialist clearance).
- Pediatric Note: In minors, the test requires written parental consent and supervision by a paediatric endocrinologist, in compliance with Federal Decree-Law No. 4 of 2016 on Medical Liability.
Patient FAQ & Clinical Guidance
1. What is the purpose of the GnRH stimulation test?
This test assesses pituitary function to diagnose hypogonadotropic hypogonadism and delayed puberty. It helps endocrinologists distinguish between hypothalamic and pituitary disorders, enabling targeted treatment with sex steroids or growth hormone when indicated.
2. How should I prepare for the test?
Overnight fasting is mandatory – you must arrive fasting to ensure accurate baseline hormone levels. Avoid strenuous exercise for 24 hours before the test. Inform our phlebotomist of all medications you are taking, as some drugs may interfere with GnRH response.
3. Are there any risks or side effects?
This test is generally safe. Rare transient reactions like mild headache or flushing may occur. Serious adverse events are extremely uncommon when performed under medical supervision. Our mobile team follows DHA emergency protocols throughout the procedure.
4. How long does the test take?
The entire procedure, including baseline blood draw, GnRH injection, and subsequent timed blood draws, typically takes 60 to 90 minutes. Results are reported within 24 hours via your preferred communication channel.
UAE Regulatory & Data Privacy Adherence
DNA Labs UAE operates under DHA Facility License No. 1143 and adheres to the highest standards of data protection and patient confidentiality. Your health information is securely processed in compliance with:
- Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL)
- Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields
- Federal Decree-Law No. 4 of 2016 on Medical Liability (governing clinical safety and patient consent)
All laboratory procedures are ISO accredited, and our mobile phlebotomy team follows UAE Ministry of Health and Prevention guidelines for home collection and cold-chain transport.
Clinical & Logistical Metadata
| Test Name | FSH and LH Stimulation by Gonadotropin-Releasing Hormone (GnRH) Test |
| Price (AED) | 750 AED |
| Turnaround Time | Same day (within 24 hours) |
| Sample Type / Matrix | Peripheral whole blood (serum) – timed baseline and post-stimulation specimens |
| Methodology Used | Chemiluminescent Immunoassay (CLIA) |
| ICD-10-CM Code | E23.0 (Hypopituitarism), E23.1 (Drug-induced hypopituitarism), E28.3 (Primary ovarian failure), E29.1 (Testicular hypofunction), R83.6 (Abnormal findings from endocrine function studies) |
| LOINC Code | 14971-5 (FSH [Units/volume] in Serum or Plasma – baseline), 15001-0 (LH [Units/volume] in Serum or Plasma – baseline), plus post-stimulation LOINC panels as applicable |
| DHA Facility License & Laboratory Address | DHA License No. 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE |
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