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Recruiting NCT06083766

NCT06083766 Metabolic and Physiologic Responses to Hormone Therapy in Transgender and Gender Diverse People

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Clinical Trial Summary
NCT ID NCT06083766
Status Recruiting
Phase —
Sponsor Mayo Clinic
Condition Effects of GAHT, on Skeletal Muscle in TGD
Study Type OBSERVATIONAL
Enrollment 24 participants
Start Date 2024-01-04
Primary Completion 2030-04

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 40 Years
Study Type OBSERVATIONAL
Interventions
hormone therapy

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 24 participants in total. It began in 2024-01-04 with a primary completion date of 2030-04.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The primary purpose of this research is to determine how gender affirming hormone therapy affects muscle physiology.

Eligibility Criteria

Inclusion Criteria: * age 18-40yrs * BMI 18.5-38 kg/m2 * Fasting glucose \< 100 mg/dL * No gender affirming gonadal surgery We seek to enroll 6 patients in each group who have been on GAHT for more than 10 months with minimal interruptions in treatment. Exclusion Criteria: * Pregnancy * Use of hormonal forms of birth control within the previous 3 months * Use of glucocorticoids, estradiol, testosterone, progestin, antiandrogens, or antiestrogens besides those received as part of a supervised hormone therapy. * Gender-affirming gonadal surgery * Prior use of gonadotropin releasing hormone (GnRH) analogues during puberty * Coronary artery disease or heart failure. * A known medical condition that in the judgment of the investigator might interfere with the completion of the protocol such as the following examples: * Inpatient psychiatric treatment in the past 6 months * Presence of a known adrenal disorder * Abnormal liver function test results (Transaminase \>2 times the upper limit of normal); testing required for subjects taking medications known to affect liver function or with diseases known to affect liver function * Abnormal renal function test results (calculated GFR \<45 mL/min/1.73m2); testing required for subjects with diabetes duration of greater than 5 years post onset of puberty * Active gastroparesis * If on antihypertensive, thyroid, anti-depressant or lipid lowering medication, lack of stability on the medication for the past 2 months prior to enrollment in the study * Uncontrolled thyroid disease (TSH undetectable or \>10 mlU/L); testing required within three months prior to admission for subjects with a goiter, positive antibodies, or who are on thyroid hormone replacement, and within one year otherwise * Abuse of alcohol or recreational drugs * Infectious process not anticipated to resolve prior to study procedures (e.g. meningitis, pneumonia, osteomyelitis). * Uncontrolled arterial hypertension (Resting diastolic blood pressure \>90 mmHg and/or systolic blood pressure \>160 mmHg) at the time of screening. * A recent injury to body or limb, muscular disorder, use of any medication, any carcinogenic disease, or other significant medical disorder if that injury, medication, or disease in the judgment of the investigator will affect the completion of the protocol (exercise testing or muscle biopsy). * Medications that may impact study end points such as mitochondrial biology e.g. beta blockers * Anti-hyperglycemic drugs including metformin * Any other medication that the investigator believes is a contraindication to the subject's participation.

Contact & Investigator

Central Contact

Jennifer R Hewlett, M.D.

✉ Hewlett.Jennifer@mayo.edu

📞 507-266-9479

Frequently Asked Questions

Who can join the NCT06083766 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 40 Years, studying Effects of GAHT, on Skeletal Muscle in TGD. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06083766 currently recruiting?

Yes, NCT06083766 is actively recruiting participants. Contact the research team at Hewlett.Jennifer@mayo.edu for enrollment information.

Where is the NCT06083766 trial being conducted?

This trial is being conducted at Rochester, United States.

Who is sponsoring the NCT06083766 clinical trial?

NCT06083766 is sponsored by Mayo Clinic. The trial plans to enroll 24 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology