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NCT Number: NCT07092527

Androgen Effects on the Reproductive Neuroendocrine Axis, 2025 Version

This research study investigates whether male-level exogenous androgens inhibit the reproductive neuroendocrine axis in otherwise healthy (non-PCOS) females.

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Key information

Age range

18 year–35 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 4

Primary location

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Transgender/Non-binary Group, Initiating Testosterone Group

  • Provision of signed and dated informed consent form
  • Stated willingness to comply with all study procedures and availability for the duration of the study
  • Aged 18-35
  • Plan to initiate testosterone therapy
  • History of regular menstrual cycles (every 24-35 days) at baseline, before beginning TRT

Inclusion criteria

Cisgender Female Group

  • Provision of signed and dated informed consent form
  • Stated willingness to comply with all study procedures and availability for the duration of the study
  • Aged 18-35
  • Having regular menstrual cycles (every 24-35 days)

Exclusion criteria

All

  • Pregnant
  • Incarcerated
  • Known cognitive impairment or institutionalized
  • Hemoglobin less than 11 gm/dl at screening evaluation
  • Weight less than 110 pounds
  • BMI <18 or >35
  • Current endocrine disease- including untreated thyroid abnormalities, pituitary or adrenal disease, polycystic ovary syndrome, or androgen producing tumor
  • Current or recent pregnancy within two months of study enrollment
  • Current or recent breast feeding within two months of study enrollment
  • Diabetes, or renal, liver, or heart disease
  • History of oophorectomy or hysterectomy
  • History of radiation or surgery involving brain structures and/or pelvis/pelvic organs
  • Currently taking any medications that may affect their reproductive hormones, such as contraceptive medications, androgens, estrogens, progestins, gonadotropin-releasing hormone (GnRH) antagonists, insulinomimetics, and metformin.
  • History of prior testosterone therapy

Treatment and study plan

Testosterone Cypionate 50 milligrams per millileter (mg/mL) Injectable Solution

Drug

Participants in the initiating group will receive weekly doses of testosterone for gender-affirming care.

Other names: Testosterone Replacement Therapy

Primary outcomes

  1. Evidence of Luteal Activity (ELA)

    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.

  2. Determination of Pulsatile Luteinizing Hormone (LH) Secretion

    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.

  3. Uterine Bleeding Pattern

    Time frame: Through study completion, an average of 7 months.

    All subjects will complete a daily uterine bleeding log using REDCap®

Secondary outcomes

  1. Evaluate Serum FSH

    Time frame: Through study completion, an average of 7 months.

    Measurement of serum follicle-stimulating hormone (FSH) levels

  2. Evaluate Serum AMH

    Time frame: Through study completion, an average of 7 months.

    Measurement of serum anti-mullerian hormone (AMH) levels

  3. Evaluate Serum LH

    Time frame: Through study completion, an average of 7 months.

    Measurement of serum luteinizing hormone (LH) levels

  4. Evaluate Serum Estradiol

    Time frame: Through study completion, an average of 7 months.

    Measurement of serum estradiol levels

  5. Evaluate Serum Testosterone

    Time frame: Through study completion, an average of 7 months.

    Measurement of serum testosterone levels

Study contacts

Contact information is provided by the study sponsor or research team.

Antoni Duleba, MD

CONTACT

[email protected]

619-804-4765

Marisa Hildebrand, MPH

CONTACT

[email protected]

619-804-4765

Sponsors and collaborators

Lead sponsor

University of California, San Diego

Other

Collaborators

  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
  • National Institutes of Health (NIH)

Registry information

Important dates

Study start
2025
Primary completion
2028
Study completion
2028
First posted
Jul 30, 2025
Registry last updated
Jan 15, 2026

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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