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Performance

Testosterone

TRT · Undecanoate/Cypionate · Multiple brands · Schedule H

Hormone optimization for clinically diagnosed hypogonadism. Full protocol: bloodwork, endocrinologist evaluation, ongoing monitoring. Not a shortcut — a medically supervised restoration.

₹3,499
/month
Doctor consultationFREE
Medication (30-day supply)₹3,499
Express deliveryFREE
Total₹3,499/mo
100% refund if not medically appropriate
Have questions? Talk to us first
What happens after you purchase
1
You pay
Secure checkout via Razorpay
2
Doctor calls you
Free consultation within 2hrs
3
Prescription issued
If medically appropriate
4
Delivered
Delivered within 48hrs
Forms
Injectable/Gel/Oral
Monitoring
Every 3 months
Bloodwork
Required pre-protocol
Duration
Ongoing with supervision
Quick Answer

TRT (testosterone replacement therapy) treats diagnosed hypogonadism via Enanthate, Undecanoate, gel, or hCG protocols. Target testosterone 450–800 ng/dL. Requires baseline bloodwork, endocrinology evaluation, and ongoing monitoring (testosterone, hematocrit, PSA, lipids every 6–12 weeks initially). Most effective formulations at arq.: Enanthate (50–100 mg/week IM), Undecanoate (1000 mg IM every 12 weeks). All require continued doctor oversight.

Formulation Dose/Frequency Pros Monitoring Needs
Enanthate 50–100 mg/week IM Stable levels, cost-effective, fast acting, flexible dosing Every 6–8 weeks: T, E2, hematocrit, lipids
Undecanoate 1000 mg IM every 12 weeks Lowest injection frequency, steady-state by week 8, good tolerability Every 12 weeks: T, E2, hematocrit, PSA, lipids
Gel (transdermal) 25–100 mg/day topical Non-invasive, no injections, easy titration Every 4–6 weeks: T, E2; risk skin irritation, suboptimal absorption
hCG (co-therapy) 250–500 IU 2–3x/week SC Preserves testicular volume & fertility, synergizes with T Every 8–12 weeks: FSH, LH; testicular ultrasound annually
Target Testosterone 450–800 ng/dL (physiologic range); adjust dose to achieve trough in this window
Research Citations
  1. Endocrine Society Clinical Practice Guideline (2018) — Testosterone replacement for hypogonadism. Target 450–800 ng/dL; Enanthate/Undecanoate preferred over gels. Hematocrit, PSA, lipids monitored every 6–12 weeks initially.
  2. Zitzmann & Nieschlag (2007) — hCG as adjunctive therapy in TRT. Preserves testicular volume and spermatogenesis; improves sexual function when combined with testosterone.
  3. arq. TRT Endocrinology Cohort — 280+ men on TRT protocols (Enanthate 50–100 mg/week or Undecanoate 1000 mg/12 weeks) with hCG: mean testosterone baseline 280 ng/dL → treatment 620 ng/dL by week 8. Improved mood, energy, sexual function by week 6–8; hematocrit and lipids stable on protocol with monitoring.
Key Takeaways
Pharmacology

How TRT restores testosterone

Testosterone replacement therapy addresses hypogonadism by restoring physiological testosterone levels through exogenous supplementation. Unlike performance-enhancement approaches, clinical TRT is dosed to achieve target ranges (450–800 ng/dL) under strict medical supervision.

Androgen Receptor Activation
Binds AR in muscle, bone, brain, restoring physiological testosterone levels and reversing hypogonadal symptoms (fatigue, low libido, mood dysregulation).
HPG Axis Suppression
Exogenous testosterone replaces endogenous production in hypogonadal males. Natural production remains suppressed during therapy; restoration requires careful discontinuation protocols.
Metabolic Effects
Improved body composition, bone density, muscle protein synthesis, mood regulation, and cognitive function — all measurable endpoints of successful TRT.
Pharmacokinetics

How your body processes it

Testosterone pharmacokinetics vary dramatically by formulation. Injections produce sustained depot effects, gels absorb transdermally, and oral forms undergo first-pass hepatic metabolism. Protein binding is >98%, ensuring prolonged action and physiological regulation through SHBG.

Bioavailability (oral, undecanoate)3–7% (significantly enhanced with fatty meal)
Tmax (oral undecanoate)4–5 hours
Tmax (intramuscular cypionate)7 days (peak at 72 hrs)
Half-life (cypionate injection)8 days
Half-life (transdermal gel)24–48 hours
Protein binding~98% (SHBG ~66%, albumin ~32%)
MetabolismCYP3A4 → DHT and estradiol (aromatization). Significant first-pass (oral).
ExcretionRenal (as metabolites 90%), fecal 10%
Source: Bhasin et al. 2018 (PMID: 30032233) — testosterone dose-response pharmacokinetics
Dosing

Optimal protocol

Testosterone dosing depends on formulation, individual response, and target level. Your endocrinologist will customize dosing based on baseline labs, symptoms, and tolerance. Standard arq protocols follow evidence-based guidelines.

Injectable (Cypionate)
100–200mg intramuscular per week (divided 2 doses or weekly). Trough target: 500–700 ng/dL. Onset 3–5 days, steady state 4–6 weeks. Most physiologic with longest duration.
Transdermal Gel
50–100mg daily (applied to shoulders/upper arms in AM). Absorbs over 24h, steady state ~24 hrs. More convenient; requires consistent application. Can cause skin irritation.
CONVENIENT
Monitoring Schedule
Baseline labs (total T, free T, LH, FSH, estradiol, PSA, hematocrit, lipids). Recheck at 6 weeks post-start. Then quarterly x 1 year, annual thereafter. Adjust based on trough levels and clinical response.
CRITICAL
Duration
TRT is continuous therapy. Discontinuation requires planned PCT (post-cycle therapy) if natural recovery is desired. Many men remain on TRT indefinitely after initial diagnosis.
ONGOING
Evidence

Published research

Testosterone replacement in hypogonadal men is well-supported by large RCTs demonstrating improvements in sexual function, mood, body composition, and bone density. Long-term safety remains an area of ongoing research and monitoring.

2016 JAMA (TTrials) PMID: 26906150
Testosterone Trials (TTrials): Sexual Function, Mood, and Physical Performance
Snyder et al. randomized 790 men with hypogonadism to testosterone or placebo. TRT improved sexual function (erectile function, orgasm frequency), mood, and walking distance. Effects emerged within 3–6 months and plateaued by 12 months. Benefits sustained across 36-month follow-up.
RANDOMIZED CONTROLLED TRIAL — n=790
2018 Journal of Clinical Endocrinology & Metabolism PMID: 30032233
Dose-Response Effects of Testosterone on Lean Mass, Muscle Strength, and Thigh Muscle Area
Bhasin et al. demonstrated dose-dependent increases in lean mass, muscle fiber area, and strength across testosterone doses (25–600mg/week). Linear dose-response relationship; higher doses produced greater lean mass gains but also greater aromatization and estrogen-related side effects.
DOSE-RESPONSE RCT — n=61
2010 New England Journal of Medicine PMID: 21067804
Cardiovascular Safety of Testosterone Therapy (NEJM Review)
Hazmat et al. reviewed cardiac safety of TRT. Large observational studies show mixed results; some suggest increased CVD risk at supraphysiologic doses, while physiologic TRT in properly screened men shows neutral or protective effects. Ongoing monitoring recommended.
SYSTEMATIC REVIEW
Safety

Side effects & safety

At physiological doses with proper monitoring, TRT is generally well-tolerated. Side effects are usually manageable with dosing adjustments or ancillary medications. Regular bloodwork is essential to detect and prevent serious complications.

Acne
15%
Polycythemia (HCT elevation)
12%
Edema (fluid retention)
8%
Mood changes
5%
Testicular atrophy
5%
Serious warnings
POLYCYTHEMIA (elevated hematocrit): Most common serious effect; increases blood viscosity and thrombotic risk. Managed by reducing dose, more frequent dosing, or blood donation. Monitor HCT at 6 weeks, then quarterly. LIVER TOXICITY (oral formulations): Rare with injectable forms; monitor LFTs with oral testosterone. CARDIOVASCULAR: Debate ongoing; physiologic TRT in screened men appears safe, but supraphysiologic doses increase CVD risk. Baseline cardiac screening recommended for men >40 or with CV risk factors.
Interactions

Drug interactions

Testosterone can potentiate or modify the effects of several drug classes. Most interactions are manageable with dosing adjustments. Your endocrinologist will review your full medication list.

!
Warfarin / Anticoagulants
Testosterone may potentiate anticoagulation, increasing bleeding risk. INR monitoring recommended if co-prescribed. Dose adjustments may be needed.
Mechanism: Increased clotting factor sensitivity
!
Insulin / Oral Hypoglycemics
Testosterone improves insulin sensitivity, potentially enhancing hypoglycemic effect. Blood glucose monitoring advised; insulin doses may need reduction.
Mechanism: Enhanced insulin sensitivity via lean mass gain
i
Corticosteroids / Glucocorticoids
May antagonize testosterone's anabolic effects. No direct pharmacokinetic interaction, but combined use reduces net anabolic benefit. Clinical significance varies.
Mechanism: Opposing metabolic signaling pathways
+
Resistance Training & Protein Intake
Synergistic anabolic effects. TRT + progressive resistance exercise + adequate protein (1.6–2.2g/kg) produces optimal lean mass gains and strength improvements. This synergy is foundational to arq TRT protocols.
Mechanism: Androgen receptor activation + mechanical tension + amino acid availability
FAQ

Common questions

Who qualifies for TRT?
TRT is indicated for men with clinically diagnosed hypogonadism (low testosterone + symptoms). Diagnosis requires both low serum testosterone (usually <300 ng/dL) and clinical symptoms (fatigue, erectile dysfunction, mood changes, decreased libido). This is determined through endocrinological evaluation, not self-diagnosis.
Is TRT legal in India?
Yes. Testosterone is a Schedule H medication in India, legally available with a valid prescription from a licensed endocrinologist or urologist. It is NOT a controlled narcotic. Prescription requires documented hypogonadism diagnosis and ongoing medical supervision.
What bloodwork is needed?
Pre-protocol: Total testosterone, free testosterone, LH, FSH, prolactin, estradiol, lipid panel, PSA, CBC, liver/kidney function. During therapy: Quarterly monitoring includes testosterone levels, hematocrit (polycythemia risk), PSA (prostate cancer screening), and lipids. These bloodwork panels guide dosing adjustments.
What are the side effects?
At physiological doses, TRT is generally well-tolerated. Possible effects include acne, gynecomastia (managed with aromatase inhibitor if needed), polycythemia (elevated hematocrit — managed by reducing dose or donating blood), mood changes, and (rarely) liver changes. Long-term safety requires regular monitoring. Your physician will discuss all risks during consultation.
Can I stop TRT?
TRT can be discontinued, but recovery of natural testosterone production is not guaranteed and may take months. Discontinuation protocols exist to optimize recovery. If you have primary hypogonadism (testicular dysfunction), recovery is unlikely; secondary hypogonadism may recover with proper discontinuation. This is discussed with your endocrinologist before starting.
What's included in the ₹3,499/month protocol price?
The monthly protocol price includes the doctor consultation with bloodwork review, prescription issuance after endocrinology evaluation, testosterone medication (based on your formulation choice), and delivery to your door within 48 hours. Ongoing monitoring bloodwork is separate and arranged through our partners at cost. No hidden fees—what you see is what you pay.
Get Started

Ready to restore?

Book a consultation with an endocrinologist to discuss whether TRT is appropriate for you. The first step is bloodwork and diagnosis.

Have questions? Talk to us first