Oregon Health and Science University
Portland, Oregon, 97239, United States
NCT Number: NCT03864913
The trial studies the efficacy of subcutaneous (SQ) testosterone compared to intramuscular (IM) testosterone therapy during the first 6 months of pubertal induction in transgender male adolescents. Describes rate of adverse effects, masculinizing effects and quality of life while receiving testosterone. Evaluates clinic utilization required for testosterone therapy.
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Notify Me14 year–19 year
Female
Interventional
Early Phase 1
Portland, Oregon, 97239, United States
Objectives:
Hypothesis: SQ testosterone results in equal or fewer adverse reactions than IM testosterone.
Hypothesis: Subjects receiving SQ testosterone will report equal or superior quality of life and satisfaction with injection technique compared to IM testosterone as SQ is less painful and easier to administer at home.
Hypothesis: Subjects using SQ testosterone will have fewer clinic visits than those using IM testosterone. This may impact healthcare-related costs.
Study Outline:
6 month study consisting of three study visits at baseline, 3 months and 6 months. Optional cross over of injection modality from 6-9 months. At each visit subjects complete blood work and questionnaires to determine testosterone peak and trough levels as well as biochemical adverse effects, quality of life, masculinizing effects and medication experience.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
SQ or IM testosterone injections for pubertal induction of transgender male adolescents. Increasing doses per protocol at 3 month and 6 month follow up.
Validated Pediatric Quality of Life questionnaire completed by subjects at baseline, 3 month and 6 month study visits.
Subjects complete self-reported questionnaire at 3 month and 6 month study visits.
Subjects complete self-reported questionnaire at 3 month and 6 month study visits.
Time frame: Two lab draws, before and after testosterone injection, drawn at 3 month and 6 month follow up
Trough and peak serum testosterone level
Time frame: Assessed at 3 month and 6 month follow up
Time frame: Completed at baseline, 3 month and 6 month follow up
Validated pediatric quality of life tool
Time frame: Completed at 3 month and 6 month follow up
Self reported, questionnaire
Time frame: Completed at 3 month and 6 month follow up
Self reported, questionnaire
Oregon Health and Science University
Other
Investigating the Efficacy of Subcutaneous Testosterone Compared to Intramuscular Testosterone in Gender Affirming Care of Transgender Male Adolescents
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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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