New study aims to freeze ovarian tissue for transgender fertility
NCT ID NCT05863676
First seen Jul 09, 2026 · Last updated Jul 10, 2026 · Updated 1 time
Summary
This study looks at how to best freeze and store ovarian tissue for transgender individuals who are undergoing gender-affirming therapy. The goal is to preserve the possibility of having biological children later. Researchers will test different freezing methods and examine how hormone treatments affect the tissue. Participants are transgender individuals with ovaries who are planning or already receiving gender-affirming hormones.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could improve fertility preservation options for transgender individuals who cannot or do not wish to undergo natal puberty.
- What could go wrong
- This is a small, early-stage study focused on tissue analysis, not on actual fertility outcomes. The techniques may not lead to successful pregnancies.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 20 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2020
- Expected to finish
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Jul 2030
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Eligible patients who will undergo gender-affirming treatments and for whom standard of care fertility preservation procedures are not available.
- Ages
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9 years and older
- Sex
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Female participants only
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria:Two Categories of participants will be eligible for this study. Category 1 participants must have all criteria listed below: * Patient with ovaries over the age of 9 * Diagnosed with gender dysphoria; currently on or imminently planning to start gender affirming treatment (hormone blockers or gender-affirming hormones) * Have a clinical referral for fertility preservation from their primary care physician * Unwilling to undergo natal puberty or, for patients who have gone through puberty, unwilling to discontinue hormone suppression and/or hormone replacement therapy. Category 2 participants only fall into this category if they are undergoing gender-affirming surgery. They must have all criteria listed below: * Patient is 18+ years old * Diagnosed with gender dysphoria * Unwilling to undergo natal puberty, or for patients who have gone through puberty, be unwilling to discontinue hormone suppression and/or sex steroid (estrogen) therapy. * Will be undergoing gender affirming surgery that involves removal of the ovaries. Exclusion Criteria: * Diagnosed with psychological, psychiatric, or other conditions which prevent giving fully informed consent. * Diagnosed with an underlying medical condition that significantly increases their risk of complications from anesthesia and surgery.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Magee-Womens Hospital
Pittsburgh, Pennsylvania, 15213, United States
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Other studies related to the condition(s) this trial covers.
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