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Completed

NCT Number: NCT03864913

Comparing Subcutaneous Testosterone to Intramuscular Testosterone in Gender Affirming Care of Transgender Male Adolescents

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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Key information

Age range

14 year–19 year

Sex eligibility

Female

Study type

Interventional

Phase

Early Phase 1

Primary location

Oregon Health and Science University

Portland, Oregon, 97239, United States

About this study

Objectives:

  • Determine the efficacy of SQ testosterone compared to IM testosterone therapy. Hypothesis: SQ testosterone is equally efficacious to IM testosterone in achieving mid-pubertal testosterone levels and masculinizing physical changes in transgender male adolescents after 6 months.
  • Determine the rate of adverse reactions of SQ and IM testosterone during the first 6 months of treatment.

Hypothesis: SQ testosterone results in equal or fewer adverse reactions than IM testosterone.

  • Evaluate quality of life (QOL) and satisfaction of injection technique for SQ and 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.

  • Evaluate and compare the number of clinical visits required for testosterone injections by transgender male patients receiving SQ and IM therapy.

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.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Testosterone naive
  • Transgender male
  • 14-19 years old

Exclusion criteria

  • Transgender males who have received testosterone therapy in the past

Treatment and study plan

Testosterone injection

Drug

SQ or IM testosterone injections for pubertal induction of transgender male adolescents. Increasing doses per protocol at 3 month and 6 month follow up.

PedsQL questionnarie

Behavioral

Validated Pediatric Quality of Life questionnaire completed by subjects at baseline, 3 month and 6 month study visits.

Masculinizing effects questionnaire

Other

Subjects complete self-reported questionnaire at 3 month and 6 month study visits.

Medication experience questionnaire

Other

Subjects complete self-reported questionnaire at 3 month and 6 month study visits.

Primary outcomes

  1. Serum testosterone level

    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

Secondary outcomes

  1. Rate of adverse effects

    Time frame: Assessed at 3 month and 6 month follow up

  2. PedsQL questionnaire score

    Time frame: Completed at baseline, 3 month and 6 month follow up

    Validated pediatric quality of life tool

  3. Masculinizing effects

    Time frame: Completed at 3 month and 6 month follow up

    Self reported, questionnaire

  4. Medication experience

    Time frame: Completed at 3 month and 6 month follow up

    Self reported, questionnaire

Sponsors and collaborators

Lead sponsor

Oregon Health and Science University

Other

Registry information

Official study title

Investigating the Efficacy of Subcutaneous Testosterone Compared to Intramuscular Testosterone in Gender Affirming Care of Transgender Male Adolescents

Important dates

Study start
2018
Primary completion
2019
Study completion
2019
First posted
Mar 6, 2019
Registry last updated
Apr 3, 2024

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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