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临床试验/NCT03864913
NCT03864913已完成早期 1 期

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

Oregon Health and Science University1 个研究点 分布在 1 个国家目标入组 26 人开始时间: 2018年1月26日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
早期 1 期
状态
已完成
入组人数
26
试验地点
1
主要终点
Serum testosterone level

研究概览

简要总结

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.

详细描述

Objectives:

  1. 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.
  2. 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. 3. 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. 4. 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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
14 Years 至 19 Years(Child, Adult)
性别
Female
接受健康志愿者

入选标准

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

排除标准

  • Transgender males who have received testosterone therapy in the past

研究组 & 干预措施

Randomized SQ vs IM

Experimental

Subjects randomized to either SQ or IM testosterone injections follow study protocol.

干预措施: Testosterone injection (Drug)

Randomized SQ vs IM

Experimental

Subjects randomized to either SQ or IM testosterone injections follow study protocol.

干预措施: PedsQL questionnarie (Behavioral)

Randomized SQ vs IM

Experimental

Subjects randomized to either SQ or IM testosterone injections follow study protocol.

干预措施: Masculinizing effects questionnaire (Other)

Randomized SQ vs IM

Experimental

Subjects randomized to either SQ or IM testosterone injections follow study protocol.

干预措施: Medication experience questionnaire (Other)

Non-randomized SQ

Experimental

Subjects choose to participate in study, but decline to randomize and select SQ injections. Follow same study protocol.

干预措施: Testosterone injection (Drug)

Non-randomized SQ

Experimental

Subjects choose to participate in study, but decline to randomize and select SQ injections. Follow same study protocol.

干预措施: PedsQL questionnarie (Behavioral)

Non-randomized SQ

Experimental

Subjects choose to participate in study, but decline to randomize and select SQ injections. Follow same study protocol.

干预措施: Masculinizing effects questionnaire (Other)

Non-randomized SQ

Experimental

Subjects choose to participate in study, but decline to randomize and select SQ injections. Follow same study protocol.

干预措施: Medication experience questionnaire (Other)

Non-randomized IM

Experimental

Subjects choose to participate in study, but decline to randomize and select IM injections. Follow same study protocol.

干预措施: Testosterone injection (Drug)

Non-randomized IM

Experimental

Subjects choose to participate in study, but decline to randomize and select IM injections. Follow same study protocol.

干预措施: PedsQL questionnarie (Behavioral)

Non-randomized IM

Experimental

Subjects choose to participate in study, but decline to randomize and select IM injections. Follow same study protocol.

干预措施: Masculinizing effects questionnaire (Other)

Non-randomized IM

Experimental

Subjects choose to participate in study, but decline to randomize and select IM injections. Follow same study protocol.

干预措施: Medication experience questionnaire (Other)

结局指标

主要结局

Serum testosterone level

时间窗: Two lab draws, before and after testosterone injection, drawn at 3 month and 6 month follow up

Trough and peak serum testosterone level

次要结局

  • Rate of adverse effects(Assessed at 3 month and 6 month follow up)
  • Masculinizing effects(Completed at 3 month and 6 month follow up)
  • PedsQL questionnaire score(Completed at baseline, 3 month and 6 month follow up)
  • Medication experience(Completed at 3 month and 6 month follow up)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Kara Connelly

Principal Investigator

Oregon Health and Science University

研究点 (1)

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