Testosterone gel vs. injections for transmasc people: what the evidence shows
Quick answer
The creator is a transgender man six days into low-dose testosterone gel therapy, who also has a pre-existing blood clotting disorder. Their prescriber appears to have selected transdermal delivery specifically to minimize supraphysiologic testosterone peaks, which are associated with greater erythrocytosis and elevated thrombosis risk compared to gel. This reflects a real clinical tradeoff in testosterone delivery selection for patients with coagulopathies.
Our take · Written by FormBlends editorial team · Reviewed by FormBlends Medical Team· This is not a transcript. It is our independent review of the video above.
What did @eddyquekett actually say?
Six days into testosterone therapy, this creator explained two reasons for choosing gel over injections: wanting slow, gradual changes with the option to stop quickly, and having a pre-existing blood clotting disorder. They said injections cause a testosterone spike that raises clot risk more than gel does, while gel keeps levels steadier. They also described their clot risk on gel as roughly equivalent to that of a cisgender man with the same disorder.
This is a remarkably specific and self-aware explanation for a TikTok video. The creator is not recommending gel to anyone else. They are describing a clinical decision made with their own prescriber, based on their own medical history. That distinction matters before we get into the science.
Does the science back this up?
Largely, yes. The pharmacokinetics argument is solid, and the clotting concern is clinically real, not invented anxiety.
Testosterone injections, particularly long-acting esters like cypionate or enanthate, produce supraphysiologic peaks in the first two to three days post-injection, followed by a trough before the next dose. Transdermal gels, by contrast, produce more stable serum testosterone concentrations day to day. This is well-documented. Bhasin et al. (2010, Journal of Clinical Endocrinology and Metabolism) confirmed that transdermal delivery attenuates the peak-to-trough swing seen with intramuscular administration.
On the clotting question, testosterone is associated with increased erythrocytosis, meaning it raises red blood cell production and hematocrit, which thickens blood and raises thrombosis risk. Guo et al. (2014, Thrombosis Research) found that supraphysiologic testosterone peaks, as seen with injections, correlate more strongly with elevated hematocrit than stable levels from transdermal routes. So the creator's reasoning is not just intuitive, it has a pharmacological basis.
What did they get right, and where does it get complicated?
They got the core pharmacology right. Where it gets more complicated is the specific claim that gel brings their clot risk to the same level as a cisgender man with the same disorder.
That is a reasonable clinical approximation, but it is not a precise statement backed by a clean dataset. Research on transgender men specifically and thrombosis risk on gel is limited. Most of what we know comes from TRT studies in cisgender men with hypogonadism, or from studies on hormone therapy in transgender populations that did not always separate delivery methods carefully.
The Nota et al. (2019, Circulation) study on transgender men and cardiovascular outcomes found that testosterone use was associated with increased cardiovascular event risk, but did not cleanly isolate gel versus injection outcomes. So saying gel puts you at exactly the risk of a cis man with the same disorder is a simplification. It may be clinically useful framing their doctor provided, but it should not be taken as a precise epidemiological fact.
The reversibility argument, stopping gel the next day versus waiting out a long-acting injection, is also accurate. Transdermal testosterone clears faster than injected esters, which can persist for days to weeks depending on the formulation.
What should you actually know?
If you have a clotting disorder and are starting testosterone, delivery method is a legitimate clinical variable worth discussing with your prescriber. This is not a niche concern.
Polycythemia, the excessive red blood cell production testosterone can trigger, is one of the most common adverse effects monitored in people on testosterone therapy. Hematocrit levels should be checked before starting therapy and monitored regularly. The Endocrine Society's 2019 clinical practice guidelines on testosterone therapy recommend monitoring hematocrit at three and six months and annually thereafter.
Route of administration does affect this. A 2020 retrospective study by Gomes et al. in the Journal of the Endocrine Society found that injectable testosterone was associated with significantly higher rates of polycythemia compared to transdermal formulations in cisgender men on TRT. This supports the gel choice for someone already at elevated clot risk.
- Gel does not eliminate clot risk, it may reduce the degree of hematocrit elevation compared to injections.
- Individual clotting disorders vary significantly. Factor V Leiden, antiphospholipid syndrome, and other conditions carry different baseline risks.
- Dose also matters. A lower dose, as the creator mentioned, further reduces the erythrocytosis signal.
- No delivery method makes testosterone risk-free for someone with a pre-existing coagulopathy. That requires specialist input, not a TikTok.
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This page currently connects to 6 source-backed evidence items through visible references or structured citation data.
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For Testosterone gel vs. injections for transmasc people: what the evidence shows, FormBlends checks the page topic against primary trials, systematic reviews, guidelines, and current PubMed-indexed literature where available. These citations are context, not medical advice, proof of eligibility, or a claim that every study applies to every patient.
Cardiovascular Safety of Testosterone-Replacement Therapy
TRAVERSE trial anchor for cardiovascular-safety discussions in appropriately diagnosed men.
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Testosterone therapy in men with androgen deficiency syndromes: an Endocrine Society clinical practice guideline
Guideline anchor for diagnosis, monitoring, contraindications, and appropriate TRT framing.
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The creator is a transgender man six days into low-dose testosterone gel therapy, who also has a pre-existing blood clotting disorder.
FormBlends verdict
The creator is a transgender man six days into low-dose testosterone gel therapy, who also has a pre-existing blood clotting disorder. Their prescriber appears to have selected transdermal delivery specifically to minimize supraphysiologic testosterone peaks, which are associated with greater erythrocytosis and elevated thrombosis risk compared to gel. This reflects a real clinical tradeoff in testosterone delivery selection for patients with coagulopathies.
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What it helps with
- The creator is a transgender man six days into low-dose testosterone gel therapy, who also has a pre-existing blood clotting disorder. Their prescriber appears to have selected transdermal delivery specifically to minimize supraphysiologic testosterone peaks, which are associated with greater erythrocytosis and elevated thrombosis risk compared to gel. This reflects a real clinical tradeoff in testosterone delivery selection for patients with coagulopathies.
- Injectable testosterone produces supraphysiologic peaks within 48 hours post-dose; transdermal gel produces significantly flatter serum levels day to day (Bhasin et al., 2010, JCEM).
- Elevated hematocrit from testosterone-driven erythrocytosis is one of the most common adverse effects monitored in testosterone therapy and is more pronounced with injections than gel (Gomes et al., 2020, Journal of the Endocrine Society).
What it may miss
- It may not cover eligibility, contraindications, medication interactions, lab history, or dose escalation.
- Compound access, legal status, and product quality still need a separate safety check.
- Social video captions rarely show the full evidence base behind a claim.
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Start provider reviewWhat You'll Learn
- Injectable testosterone produces supraphysiologic peaks within 48 hours post-dose; transdermal gel produces significantly flatter serum levels day to day (Bhasin et al., 2010, JCEM).
- Elevated hematocrit from testosterone-driven erythrocytosis is one of the most common adverse effects monitored in testosterone therapy and is more pronounced with injections than gel (Gomes et al., 2020, Journal of the Endocrine Society).
- Nota et al. (2019, Circulation) found transgender men on testosterone had higher rates of cardiovascular events than cisgender women, but the study did not isolate delivery method as a variable cleanly.
- The Endocrine Society recommends checking hematocrit before testosterone initiation and at 3, 6, and 12 months, especially in patients with pre-existing clotting conditions.
- Stopping gel the day after application clears the dose faster than waiting out an injected ester, which can persist in circulation for days to over a week depending on formulation.
- A pre-existing blood clotting disorder is a legitimate clinical factor in choosing testosterone delivery route, and this conversation belongs with a prescriber who knows the specific diagnosis, not a general recommendation for all trans men.
- Low-dose testosterone combined with transdermal delivery is a real harm-reduction strategy for at-risk patients, not just a preference issue.
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About the Creator
Eddy 🌱 · TikTok creator
31.7K views on this video
Replying to @jesseykamp Why I'm on Testosterone gel rather than injections! #Transgender #Trans #Queer #Transmasc #Testosterone #ftm
Sources & references
Citations extracted from our medical team's review. Click any citation to search PubMed.
Not medical advice. This video was made by Eddy 🌱, not by FormBlends. Our write-up above is an editorial review, not a medical recommendation. Talk to your doctor before making any decisions about medications or treatments.