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Muscle & performance

Testosterone (TRT)

TRT · Testosterone replacement therapy · Testosterone cypionate · Testosterone enanthate

ApprovedProhibited in sportReviewed 18 Aug 2026

Testosterone is a steroid hormone, not a peptide. It is on this site because people track it alongside everything else here, and because the most important fact about it, that it suppresses your own production and your fertility, is the one most likely to be discovered too late.

As replacement therapy for diagnosed hypogonadism it is well-evidenced approved medicine, and for men who genuinely have low testosterone confirmed on repeat morning bloodwork, it works: energy, mood, libido, bone density, body composition. That is a real treatment for a real diagnosis.

The gap between that and how it is actually obtained is wide. Online clinics prescribe from a single blood draw and a symptom questionnaire, when diagnosis requires at least two morning measurements plus an assessment of why levels are low. Symptoms of low testosterone are also the symptoms of poor sleep, obesity, depression and thyroid disease, and some of those are reversible in a way that starting lifelong therapy is not.

Two things are worth knowing before starting. It suppresses your own production, and after prolonged use recovery is uncertain and can take a year or more. And it stops sperm production in most men, which is reversible for many and not for all. Neither is a side effect at the margin; both are what the drug does.

How it works

Testosterone binds the androgen receptor, driving protein synthesis, red blood cell production, bone density and the range of effects associated with male physiology.

Some converts to oestradiol via aromatase, and that matters. Oestradiol in men is necessary for bone and libido, and both too little and too much cause problems. This is why aromatase inhibitors are commonly over-used alongside it.

Some converts to dihydrotestosterone via 5-alpha reductase, which drives prostate and scalp effects.

Exogenous testosterone suppresses GnRH, LH and FSH through negative feedback. Without LH the testes stop producing their own; without FSH sperm production stops. This is the mechanism behind both testicular atrophy and infertility, and it is not avoidable by dosing carefully.

Regulatory status — United States

Approved by the FDA and EMA for diagnosed male hypogonadism, and a Schedule III controlled substance in the United States. Labelling was updated in 2025 following the TRAVERSE trial. Not approved for age-related decline in testosterone without a confirmed diagnosis.

Last reviewed 18 Aug 2026. Regulatory positions in this category change frequently; we date this line so you can see how current it is.

What it is studied for

Each entry states the evidence behind it. We do not rank indications by effectiveness — for most compounds here, that would be a claim nobody can support.

Diagnosed male hypogonadism

Published review

The approved indication.

EvidenceExtensive trial evidence for improvements in sexual function, mood, bone density and body composition in men with confirmed low testosterone.

Cardiovascular safety

Clinical trial

A long-standing question, now largely answered.

EvidenceThe TRAVERSE trial, in men with hypogonadism and cardiovascular risk, found testosterone therapy non-inferior to placebo for major adverse cardiac events. It also found higher rates of atrial fibrillation, pulmonary embolism and acute kidney injury.

Performance and body composition in men with normal levels

Clinical trial

Not an approved use.

EvidenceSupraphysiological testosterone increases muscle mass and strength. That is not in doubt. It is also not replacement therapy, and the risk profile is different.

Identity and clearance

Molecule

Class
Steroid hormone, not a peptide
Molecular weight
288.4 Da

Included here because it is tracked alongside peptides, not because it belongs to the same class.

Dose protocols reported in sources

Displayed for reference only. Every row says where it came from, and a trial protocol and a community convention are not the same kind of information. None of this is fed into the calculator, and none of it is a recommendation.

Dose protocols reported in sources, with the source of each.
GoalDoseFrequencyRouteUnitsSourceStart this protocol
Replacement therapy, injectable ester50 mg – 100 mgWeekly, or split twice weeklyIntramuscular50 to 100 mg per week is the usual replacement range for cypionate or enanthate, titrated against trough total testosterone, haematocrit and oestradiol. Splitting the dose gives steadier levels. The figures here are in micrograms for consistency with the rest of the site; every clinical source uses milligrams.Published reviewStart this

Start this copies a row into a protocol of your own, which you can then edit. Where a source gave a dose range or an ambiguous frequency, those fields arrive empty — we will not pick a number on your behalf.

Safety

Reported effects

  • Suppression of your own productionPublished review

    Universal

    Not a side effect so much as the mechanism. Recovery after prolonged use is uncertain and can take a year or longer.

  • InfertilityPublished review

    Most men, while taking it

    FSH suppression stops sperm production. Often reversible, not always, and less so the longer it has been going on. If you may want children, discuss this before starting rather than after.

  • Raised haematocritPublished review

    Common

    Thickened blood raises clot risk. This is the single most important thing routine bloodwork is looking for, and it is manageable when someone is checking.

  • Testicular atrophyPublished review

    Common

  • Acne and oily skinPublished review

    Common

  • GynaecomastiaPublished review

    Common

    From aromatisation to oestradiol. Managed by dose adjustment, and over-suppressing oestradiol with an aromatase inhibitor causes its own problems: joint pain, low libido, bone loss.

  • Atrial fibrillation, pulmonary embolism and acute kidney injuryClinical trial

    Higher than placebo in TRAVERSE

    The same trial that established cardiovascular non-inferiority found these raised. Both findings belong together.

  • Worsening sleep apnoeaPublished review

    Reported

  • Mood changes and irritabilityPublished review

    Reported

When to stop

  • Chest pain, breathlessness, or leg pain and swelling. Clot symptoms. Seek emergency care.
  • Haematocrit above the range your clinician set. This needs a dose change or a blood donation, not waiting.
  • Breast tenderness or enlargement.
  • Severe mood changes, aggression or worsening depression.
  • Worsening snoring or daytime sleepiness. Sleep apnoea.
  • Reduced urine flow or difficulty passing urine.

Interactions and situations that need care

  • Prostate or breast cancerAvoid

    Testosterone drives growth in hormone-sensitive tissue. An absolute contraindication in the prescribing information.

  • Wanting to conceive, now or laterAvoid

    It stops sperm production in most men. Recovery is common but not guaranteed, and becomes less likely with longer use. Sperm banking before starting is the standard advice and is easy to arrange beforehand and impossible afterwards.

  • Untreated severe sleep apnoeaAvoid

    Testosterone can worsen it, and severe untreated apnoea carries its own cardiovascular risk.

  • Raised haematocrit or polycythaemiaAvoid

    It raises red cell mass further. This is the most common reason therapy is paused, and it needs monitoring rather than judgement.

  • Women, and anyone who is pregnantAvoid

    Causes virilisation, and is harmful to a developing fetus. Note that gels transfer by skin contact, which has caused virilisation in partners and children.

  • Starting without repeat morning bloodwork and a diagnosisAvoid

    Diagnosis needs at least two morning measurements and an assessment of why levels are low, because the symptoms overlap almost entirely with poor sleep, obesity, depression and thyroid disease. Some of those are reversible. Starting testosterone is close to permanent. It suppresses what it replaces, so stopping means recovering over many months, or not fully recovering. A clinic that prescribes from one draw and a questionnaire has skipped the part that decides whether this is the right treatment.

  • Competing in a tested sportAvoid

    WADA class S1, prohibited at all times, and testing for it is routine and long established.

SportProhibited by the World Anti-Doping Agency under S1: Anabolic Agents, at all times, in and out of competition. Testing for exogenous testosterone is long established and routine, including isotope-ratio methods that distinguish it from what the body makes.

What to expect

  • For diagnosed hypogonadism this works and is well evidenced. That is not the same as it being right for low-normal levels and tiredness.
  • It stops sperm production in most men. Bank sperm before starting if children are a possibility.
  • It suppresses your own production. Coming off after years means an uncertain recovery measured in months.
  • TRAVERSE settled the cardiovascular question in the reassuring direction, and found raised atrial fibrillation, pulmonary embolism and kidney injury. Both halves are the result.
  • Haematocrit is the number that most often forces a change. Without bloodwork you will not know it has risen.
  • It is not a peptide. It is on this site because people track it here, and because the fertility consequence is the one most often learned too late.

Storage and handling

Freeze-dried powder
Supplied as an oil solution, not a powder. Store at room temperature, away from light.
After mixing
Nothing to reconstitute. A multi-dose vial is good until its expiry if the stopper is cleaned before each draw.
Long-term, frozen
Do not refrigerate or freeze. The oil thickens and crystals form.

Printable one-pagerHow to reconstitute a vial, step by step

With other peptides

  • HCGsynergistic

    The standard pairing. hCG replaces the pituitary signal that testosterone suppresses, maintaining testicular size and sperm production. Normally prescribed together rather than added independently.

  • Gonadorelinsynergistic

    Used for the same purpose as hCG, acting on the pituitary instead of the testes. Which one suits depends on where the suppression sits, which is a clinical question.

  • MK-677caution

    Both cause fluid retention, and MK-677 also worsens insulin sensitivity. The combination compounds oedema and metabolic effects.

Check this against a whole stack

Checking your vial

Research chemicals carry no manufacturing standard, so what the vial looks like is often the only quality signal available before you use it. More on assessing quality and COAs.

  • Clear oil solution, faintly yellow

    Normal. Cypionate and enanthate are dissolved in cottonseed or sesame oil.

  • Visible crystals

    Usually from being stored cold. Warming the vial in the hand normally redissolves them.

  • No manufacturer packaging, lot number or expiry

    Underground-lab testosterone is common and inconsistently dosed. There is no way to assess it by eye.

Questions

Will it make me infertile?
It stops sperm production in most men while taken. That is often reversible after stopping, and less reliably so the longer it has been going on. hCG alongside it substantially reduces the problem. If children are a possibility, bank sperm before starting. It is straightforward beforehand and not an option once suppression is established.
Can I stop once I start?
You can, and your own production will be suppressed when you do. Recovery typically takes months and is not guaranteed after years of use. This is why the diagnosis matters so much more than it seems at the point of starting.
Is it bad for the heart?
The TRAVERSE trial found testosterone non-inferior to placebo for major adverse cardiac events in men with hypogonadism and cardiovascular risk, which was reassuring. The same trial found higher rates of atrial fibrillation, pulmonary embolism and acute kidney injury. Anyone citing only one of those results is selling something.
Why is a steroid on a peptide site?
Because people track it alongside peptides, and because leaving it out would mean the fertility consequence goes unstated in the one place someone might read it before starting.

References

  1. Testosterone cypionate and enanthate: FDA prescribing information

    US Food and Drug Administration, 2025 · Regulatory label

    Men with diagnosed hypogonadism · Titrated against trough total testosterone

    Approved for diagnosed male hypogonadism. Contraindicated in prostate or breast cancer. Warnings cover polycythaemia, sleep apnoea, suppression of spermatogenesis, and secondary exposure from topical formulations. Schedule III in the United States. Labelling was revised in 2025 following the TRAVERSE results.

  2. Cardiovascular safety of testosterone-replacement therapy (TRAVERSE)

    New England Journal of Medicine, 2023 · Randomised, double-blind, placebo-controlled non-inferiority trial

    5,246 men aged 45 to 80 with hypogonadism and cardiovascular disease or high risk · Transdermal testosterone gel, titrated

    Testosterone was non-inferior to placebo for major adverse cardiac events. Higher incidences of atrial fibrillation, acute kidney injury and pulmonary embolism were observed in the testosterone group.

    10.1056/NEJMoa2215025

  3. Community and clinic practice, unverified

    Forums, coaching protocols and wellness-clinic marketing, 2026 · Anecdote

    Self-selected, unverified

    Doses and schedules described outside medical supervision. No study design — no adverse event capture — and heavy selection bias.

Keep this page honest

If something here is wrong, out of date, or missing a source, tell us and we will fix it and say that we did.

Suggest a correction

This page is educational. It describes what published research reports, not what you should do. Peptides discussed here are largely not approved for human use, and nothing on Bioalmanac is medical advice. No clinician reviews these pages.

Page last updated 18 Aug 2026