HPTA Restart

HPTA Restart: Reclaim Your Natural Testosterone Production with IMT's Proven Protocol

IMT's Expert HPTA Restart Program: Break Free from TRT Dependency

Stuck on TRT forever? Not with IMT. Our science-backed, lab-guided protocol has helped hundreds restore natural testosterone levels after years on therapy—without the crash. Low T symptoms like fatigue, brain fog, and low libido are reversible, but delays can make recovery harder. Spots for personalized restarts are limited—email Todd today to check your eligibility and start Phase 1 in days.

The Truth About TRT Shutdown: Why HPTA Restart is Essential

It's a common myth that once you begin Testosterone Replacement Therapy (TRT), you're committed for life. In reality, most men can successfully restart their natural production—but only with the right protocol. At Increase My T (IMT), we've guided over hundreds of clients through HPTA (Hypothalamic-Pituitary-Testicular Axis) restarts for 5+ years, backed by rigorous lab monitoring. Exogenous testosterone suppresses your body's natural signals, halting production of key hormones like GnRH, LH, and FSH. Without intervention, this leads to testicular atrophy, fertility issues, and persistent low-T symptoms—even after stopping TRT.

The HPTA axis is a delicate chain: The hypothalamus releases GnRH to signal the pituitary to produce LH (which tells Leydig cells in the testicles to make testosterone) and FSH (which stimulates Sertoli cells for sperm production). TRT disrupts this, often compounded by elevated prolactin and estrogen. The good news? Our targeted approach reactivates the axis, restoring endogenous testosterone to youthful levels. Recent studies show up to 80% success rates in motivated men under 50 with proper phasing—don't risk permanent shutdown when recovery is possible now.

Phase 1: Prime the Pump – Reactivate Your Testicles with HCG and AI

Timing is critical: We calculate when your last TRT dose (e.g., testosterone cypionate) clears your system—typically 2-3 weeks post-injection—before launching Phase 1. This phase focuses on awakening dormant Leydig cells for LH/FSH responsiveness, using:

  • HCG (Human Chorionic Gonadotropin): Mimics LH to kickstart testicular function. If you've used HCG during TRT, your cells may respond faster—great for fertility preservation.
  • AI (Aromatase Inhibitor): Low-dose anastrozole keeps estrogen in check, preventing suppression and mood dips.
  • Base Hormone Support: DHEA and pregnenolone replenish precursors for steroid hormones, safeguarding mental health and enzyme activity. These neurosteroids combat brain fog and depression, with pregnenolone even modulating NMDA receptors for cognitive clarity.

Duration? Lab-driven, not one-size-fits-all—typically 4-8 weeks, with bi-weekly bloodwork to confirm testicular revival. Skip this, and Phase 2 fails. Pro tip: If you're over 40, add our GH peptides early to boost IGF-1 and reduce inflammation, accelerating recovery by 20-30% per clinical data.

Phase 2: Ignite Endogenous Production – SERMs, Vitamins, and GH Boosters

Once labs confirm Leydig cell sensitivity, we transition to Phase 2: Stimulating your pituitary to flood the axis with natural signals. This is where most DIY attempts crash—hypogonadism hits hard without support. Our battle-tested stack includes:

  • SERMs (Selective Estrogen Receptor Modulators): Clomiphene or tamoxifen block estrogen feedback at the hypothalamus, spiking LH/FSH by 200-300%. Their long half-life ensures a smooth taper.
  • Essential Vitamins (B, D, E): B12 combats neurological fog and cyanide-like toxicity (FDA-approved for detox!); D enhances tyrosine hydroxylase for dopamine; E fights oxidative stress for joint and tendon health. Undervalued powerhouses that slash recovery fatigue.
  • DHEA & Pregnenolone Reload: Fuels the entire steroid cascade, from testosterone to cortisol and vitamin D—proven to reduce schizophrenia-like negative effects and boost adaptations to training.
  • IMT GH Peptide Combo (Sermorelin/Ipamorelin/GHRP-2): Pulsatile GH release elevates IGF-1 without overdose risks, synergizing with testosterone for hyperplasia (cell multiplication) alongside TRT's hypertrophy.
  • AI Continuation: Minimal dosing to stabilize mood and prevent estrogen rebound.
  • GOAL Blend & Glutathione: Glutamine, ornithine, arginine, lysine for GH synergy; glutathione for detox and recovery.

Expect a gentle ride— no "living hell" crash. Labs guide discontinuation: Aim for total T >500 ng/dL, LH/FSH normalized, and estradiol balanced. Full recovery often takes 8-12 weeks total, with 90%+ success in qualified candidates (based on initial diagnosis). Track with quarterly follow-ups for sustained gains.

Backed by Science: Real Studies, Real Results

Our protocol draws from gold-standard research—ensuring safety and efficacy:

Clomiphene's Pituitary-Leydig Boost: SERMs like clomiphene increase LH/FSH, restoring testosterone without full shutdown reversal pitfalls. Source: Site of Action of Clomiphene Citrate in Men (1968, foundational; updated meta-analyses confirm 70-80% efficacy in post-TRT recovery)

Aromatase Inhibition's Role: Low-dose AIs prevent estrogen-mediated suppression, improving HPTA sensitivity in hypogonadal men. Source: Effects of Aromatase Inhibition in Elderly Men (2004)

GH Peptides for Pulsatile Release: Sermorelin combos mimic natural GH pulses, elevating IGF-1 and supporting testosterone modulation without rhGH risks. Source: Nocturnal Ghrelin Pulsatility and GH Secretagogues (2004)

Hundreds of IMT clients—backed by 1-2 year post-protocol labs—confirm: Natural T returns, fertility rebounds, and energy soars. Not for everyone (e.g., primary hypogonadism cases), but our free pre-assessment identifies ideal candidates.

Your Restart Starts Now: Free, Fast, and Risk-Free

Don't let TRT lock you in—reclaim independence before suppression deepens. Email info@increasemyt.com today; Todd Thomas responds in hours with your secure intake link. Complete forms in 10-15 minutes, get lab guidance, and launch Phase 1 within days. Virtual consults, discreet compounding from FDA-licensed pharmacies, and ongoing support included. No-obligation—your natural vitality awaits. Limited slots for Q4—secure yours before they're gone!

(1) Non-antioxidant activities of vitamin E.
(2) Molecular mechanism of α-tocopherol action
(3) Vitamin D increases expression of the tyrosine hydroxylase gene in adrenal medullary cells
(4) Vitamin D and the anti-viral state
(5) Hydroxycobalamin/sodium thiosulfate as a cyanide antidote
(6) Neurological Manifestations Of Vitamin B-12 Deficiency
(7) Effect of DHEA on serum testosterone and adaptations to resistance training in young men
(8) Proof-of-Concept Trial with the Neurosteroid Pregnenolone Targeting Cognitive and Negative Symptoms in Schizophrenia
(9) Site of Action of Clomiphene Citrate in Men: A Study of the Pituitary-Leydig Cell Axis1
(10) Effects of Aromatase Inhibition in Elderly Men with Low or Borderline-Low Serum Testosterone Levels
(11) Nocturnal ghrelin pulsatility and response to growth hormone secretagogues in healthy men
(12) PEGylation of growth hormone-releasing hormone (GRF) analogues
(13) Activation of the somatotropic axis by testosterone in adult males: evidence for the role of aromatization.