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Recovery Is Not Optional

Your HPTA recovery protocol generated from your actual cycle details. Clearance timing, SERM dosing, and support compounds. Not a forum copy-paste.

Input Your Cycle
Longer cycles cause deeper HPTA suppression. Be accurate.
Select every compound from this cycle. The longest-acting ester sets your clearance window.
Short Esters — Clear in Days
Long Esters — Clear in Weeks
Oral Only — Clear Rapidly (1-3 Days)
Ultra-Long — Clear in Months
HCG on cycle maintains Leydig cell function. This changes the recovery protocol.
Yes
No
Leydig cell desensitization likely occurred. HCG loading phase is warranted before SERM therapy.
Recovery potential declines with age. This is pharmacology, not willpower.
Cumulative HPTA stress compounds. Recovery slows with each successive cycle.
Protocol Assessment

Cycle Severity Classification

Visual Timeline

Your PCT Timeline

Phase 1
Phase 3
Phase 4
Phase 5
A protocol framework, not a prescription. Individual recovery varies based on genetics, health, and adherence. Monitor bloodwork and adjust. If LH/FSH remain suppressed 12 weeks post-PCT, see an endocrinologist. Educational purposes only. Not medical advice.
SERM efficacy for HPTA recovery: Tamoxifen at 20mg/day has been shown to restore LH levels to baseline within 2-6 weeks in most male subjects with suppressed gonadotropins. Clomiphene citrate stimulates both LH and FSH release via hypothalamic estrogen receptor antagonism. Based on published HPTA recovery data and clinical endocrinology literature.
HCG pre-loading rationale: HCG at 1000-1500 IU every other day maintains intratesticular testosterone concentrations and preserves Leydig cell responsiveness during exogenous androgen use. This pre-loading strategy ensures that when SERMs stimulate endogenous LH production, the Leydig cells are capable of responding with testosterone synthesis. Based on published data on HCG and intratesticular testosterone maintenance.
19-nor metabolite suppression: Nandrolone and trenbolone metabolites (particularly 19-norandrosterone) can remain detectable and suppressive to the HPTA for extended periods — up to 18 months for nandrolone decanoate in some individuals. This is due to the lipophilic nature of 19-nor metabolites sequestering in adipose tissue and slowly releasing. Based on pharmacokinetic data from anti-doping literature and clinical HPTA recovery studies.
Age and HPTA recovery: Men over 40 demonstrate 30-40% slower recovery of gonadotropin function compared to men under 30 following exogenous androgen suppression. This is attributable to age-related decline in hypothalamic GnRH pulse generator sensitivity and reduced Leydig cell reserve. Based on published endocrinology literature on age-related hypogonadism and HPTA function.
Clearance time calculation: Approximately 5 half-lives are required for a compound to reach less than 3.125% of its peak concentration — the threshold below which HPTA recovery can meaningfully begin. This is a standard pharmacokinetic principle applied across all drug classes.
Dual-SERM approach: Combining tamoxifen and clomiphene in severe suppression cases leverages complementary mechanisms — tamoxifen provides potent estrogen receptor antagonism at the breast and hypothalamus, while clomiphene additionally stimulates FSH release supporting spermatogenesis recovery. Based on clinical protocols used in male hypogonadism treatment literature.

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