Gender Dysphoria Clinical Trial
Official title:
Ovarian Tissue Cryopreservation in the Setting of Gender-affirming Therapy
NCT number | NCT05863676 |
Other study ID # | STUDY19060046 |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | July 14, 2020 |
Est. completion date | July 2030 |
The goal of this study is to learn about fertility preservation in the gender-diverse community. The main objectives it aims to understand are to: 1. To optimize techniques for cryopreservation of ovarian tissues, including determining efficacy of cryopreservation techniques. 2. To investigate factors affecting ovarian tissue and follicles, such as previous treatment with leuprolide acetate, or hormone therapy
Status | Recruiting |
Enrollment | 20 |
Est. completion date | July 2030 |
Est. primary completion date | July 2030 |
Accepts healthy volunteers | |
Gender | Female |
Age group | 9 Years and older |
Eligibility | 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. |
Country | Name | City | State |
---|---|---|---|
United States | Magee-Womens Hospital | Pittsburgh | Pennsylvania |
Lead Sponsor | Collaborator |
---|---|
University of Pittsburgh |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | To optimize techniques for cryopreservation of ovarian tissues, including determining efficacy of cryopreservation techniques. | Without undergoing puberty in one's natal sex, there are no standard of care fertility preservation options available for these patients. The study will aim to optimize techniques for cryopreservation of ovarian tissues by utilizing the best scientific standards for cryopreservation. | [10 years] | |
Primary | To investigate factors affecting ovarian tissue and follicles, such as previous treatment with leuprolide acetate, or hormone therapy. | For transgender male patients, medical treatment is primarily comprised of testosterone, which is often preceded by GnRH agonists (such as leuprolide acetate) to reduce endogenous estrogen production. There are theoretical concerns about the effects of long-standing hormonal treatment on the gonads and future fertility potential. The study aims to determine whether factors such as gender-affirming treatment affects the ovarian tissue and follicles by examining tissue donated to research. | [10 years] |
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