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Free Testosterone Test -
Measures free testosterone to diagnose hormonal imbalances, causing fatigue
Synonym Free Testosterone Test
Test Code ENDT26040054
Test Type Endocrinology
Pre-Test Condition Fasting
Report Availability 1–2 D(s)
# Test(s) 1
Test details Sample Report
Free Testosterone Test Sample Report Cowin-PathLab
Synonym Free Testosterone Test
Test Code ENDT26040054
Test Category Hormonal Imbalances
Pre-Test Condition Fasting
Medical History Share & see Test Details
Report Availability 1–2 D(s)
Specimen/Sample Refer Test Details
Stability @21-26 deg. C 8 H(s)
Stability @ 2-8 deg. C 7 D(s)
Stability @ Frozen 6 M(s)
# Test(s) 1
Processing Method Biochemistry
Overview: Free Testosterone Test
Introduction: The Free Testosterone Test measures free testosterone to diagnose hormonal imbalances, causing fatigue. Aligned with 2023 AUA guidelines, it uses biochemical methods for high specificity, supporting hormonal screening. This test is critical for guiding diagnosis, treatment planning, and improving outcomes in endocrinology for patients with suspected hormonal imbalances.
Other Names: Free Testosterone Assay, Unbound Testosterone Test.
FDA Status: Laboratory-developed test (LDT), meeting endocrinology standards for diagnostic accuracy.
Historical Milestone: Free testosterone testing began in the 1980s with hormonal research. Biochemical methods improved in the 2000s, enhancing diagnostic precision.
Purpose: Measures free testosterone to diagnose hormonal imbalances, guides treatment, and evaluates patients with fatigue.
Test Parameters: 1. Free Testosterone Level
Pretest Condition: Fasting for 10-12 hours required. Collect serum, plasma, or saliva. Report history of fatigue or hormonal symptoms.
Specimen: Serum (SST, 2-5 mL), Plasma (EDTA, 2-4 mL), Saliva (sterile container, 1-2 mL). Transport in a biohazard container.
Sample Stability at Room Temperature: 8 hours
Sample Stability at Refrigeration: 7 days
Sample Stability at Frozen: 6 months
Medical History: Document fatigue, low libido, or history of hormonal imbalances. Include current medications, especially testosterone therapy.
Consent: Written consent required, detailing the tests purpose, hormonal imbalance implications, and risks of sample collection.
Procedural Considerations: Uses enzyme-linked immunosorbent assay (ELISA) or chemiluminescence to measure free testosterone levels. Results are available in 1-2 days, supporting clinical decisions. Performed in laboratories, often for hormonal imbalance diagnosis.
Factors Affecting Result Accuracy: Improper fasting or sample hemolysis can affect results. Medications like anabolic steroids may alter testosterone levels.
Clinical Significance: Abnormal free testosterone confirms hormonal imbalances, guiding testosterone therapy. Normal levels may require SHBG or LH testing.
Specialist Consultation: Consult an endocrinologist or urologist for result interpretation and treatment planning.
Additional Supporting Tests: Total testosterone, SHBG, or LH/FSH to confirm hormonal imbalance diagnosis.
Test Limitations: Non-specific for certain hormonal conditions; clinical correlation is needed. Sample quality affects sensitivity.
References: AUA Testosterone Guidelines, 2023; Journal of Clinical Endocrinology, Rosner W, 2022.

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