University of California, San Diego
San Diego, California, 92037, United States
Location status: Recruiting
Location contact
Antoni Duleba, MD
CONTACT
Marisa Hildebrand, MPH
CONTACT
NCT Number: NCT07092527
This research study investigates whether male-level exogenous androgens inhibit the reproductive neuroendocrine axis in otherwise healthy (non-PCOS) females.
Interested in participating?
Request Info18 year–35 year
Female
Interventional
Phase 4
San Diego, California, 92037, United States
Location status: Recruiting
Antoni Duleba, MD
CONTACT
Marisa Hildebrand, MPH
CONTACT
Testosterone Replacement Therapy (TRT) is the mainstay of gender affirming care for transgender men (TGM) who have male gender identity after female sex assignment at birth. TGM receiving TRT over time exhibit irregular menstrual bleeding, however, the mechanism of menstrual disruption is unknown. Therefore, the investigators propose to evaluate the effect of chronic testosterone (T) exposure on ovarian hormones and pituitary gonadotropin release that determines menstrual cyclicity. The investigators will conduct a detailed study of blood reproductive hormone secretion in TGM before and during TRT as well as in untreated cisgender female (CGF) control subjects who report female gender identity congruent with female sex assignment at birth. The investigators will also perform periodic clinical and ultrasonographic evaluations.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Transgender/Non-binary Group, Initiating Testosterone Group
Inclusion criteria
Cisgender Female Group
Exclusion criteria
All
Participants in the initiating group will receive weekly doses of testosterone for gender-affirming care.
Other names: Testosterone Replacement Therapy
Time frame: Through study completion, an average of 7 months.
Evidence of Luteal Activity (ELA), as defined by serum progesterone level above 3 ng/mL in transgender men initiating testosterone replacement therapy.
Time frame: Through study completion, an average of 7 months.
Subjects will have baseline measurement of serum LH immediately followed by frequent blood sampling at 10-min intervals for 8 h. We will measure LH pulse frequency, the number of LH pulses per 8 hours.
Time frame: Through study completion, an average of 7 months.
All subjects will complete a daily uterine bleeding log using REDCap®
Time frame: Through study completion, an average of 7 months.
Measurement of serum follicle-stimulating hormone (FSH) levels
Time frame: Through study completion, an average of 7 months.
Measurement of serum anti-mullerian hormone (AMH) levels
Time frame: Through study completion, an average of 7 months.
Measurement of serum luteinizing hormone (LH) levels
Time frame: Through study completion, an average of 7 months.
Measurement of serum estradiol levels
Time frame: Through study completion, an average of 7 months.
Measurement of serum testosterone levels
Contact information is provided by the study sponsor or research team.
Antoni Duleba, MD
CONTACT
Marisa Hildebrand, MPH
CONTACT
University of California, San Diego
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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