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Testosterone Therapy With or Without Finasteride After Spinal Cord Injury: TRT-SCI Trial (TRT-SCI)

2026年8月3日 更新者:VA Office of Research and Development

A Multisite, Double-blind, Randomized Controlled Trial Comparing Body Composition, Muscle, and Bone Changes to TestosteRone Therapy With or Without Finasteride After Spinal Cord Injury: TRT-SCI Trial

Spinal cord injury (SCI) results in lower limb muscle loss, bone loss, and high fat mass that impede the recovery of physical function, increase bone fracture risk, and worsen health and quality of life. These deficits result from reduced activity after SCI and may be worsened by low testosterone, which is present in many men with SCI. In older men with low testosterone who do not have SCI, testosterone therapy (TRT) is known to increase muscle mass, muscle strength, and bone mineral density, and to reduce body fat. However, it is not known if TRT is effective in men with SCI. The purposes of this study are to determine the effectiveness of TRT in men who have low testosterone and difficulty walking after chronic motor incomplete SCI and to assess whether a process in the body that changes testosterone to dihydrotestosterone (DHT; another hormone that is stronger than testosterone) impacts the effectiveness of TRT in the impaired lower limbs and in other tissues after SCI. The researchers hypothesize that TRT will improve muscle and bone in the impaired limbs of men with chronic incomplete SCI and reduce fat mass, and that finasteride (a drug that blocks that blocks a process that changes testosterone to DHT) will influence prostate symptoms but not the musculoskeletal or body composition benefits produced by TRT.

研究概览

详细说明

There is no known cure for spinal cord injury (SCI) nor for the muscle, bone, or metabolic deficits that impair physical function, increase fracture risk, and worsen health after SCI. These deficits are preceded by the neural insult and impaired motor function and may be impacted by low testosterone, present in many men with SCI. Testosterone therapy (TRT) is known to improve musculoskeletal health, body composition, and physical function in older men with low testosterone who do not have SCI and some of the effects of TRT are known to be mediated by the 5-alpha reductase type II (5AR2) enzyme, which converts testosterone to dihydrotestosterone (DHT; a more potent endogenous metabolite). However, it remains unknown whether TRT improves muscle mass, muscle function, bone mineral density, and body composition / metabolic health in men with low testosterone and ambulatory dysfunction after chronic incomplete SCI, and whether actions of 5AR2 mediates any of the effects of testosterone in the impaired lower limbs and in other tissues with reduced neural input after SCI.

For this study, men with low testosterone and ambulatory dysfunction after chronic motor incomplete SCI will be randomized to receive TRT with or without the 5AR2-inhibitor finasteride or a placebo treatment for 9 months. TRT or placebo injection will be administered every other week; finasteride or placebo will be administered daily. Participants will be assessed at study entry and regularly thereafter. Assessments will include measurements of body composition and bone mineral density by dual energy x-ray absorptiometry (DXA) scans, bone microstructure and strength by high-resolution peripheral quantitative computerized tomography (HR-pQCT) scans, and tests of muscle strength and physical function. Participants will also undergo safety tests, including electrocardiogram (ECG) for cardiac electrophysiology, questionnaires of health status, and blood tests to assess prostate specific antigen (PSA), hematocrit, liver enzymes (AST and ALT), blood lipids, sex hormones, and other markers of health.

研究类型

介入性

注册 (估计的)

300

阶段

  • 阶段2
  • 第三阶段

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

学习地点

    • Colorado
      • Aurora、Colorado、美国、80045-7211
        • Rocky Mountain Regional VA Medical Center, Aurora, CO
        • 接触:
        • 首席研究员:
          • Joshua F Yarrow, PhD MS BS
    • Florida
      • Gainesville、Florida、美国、32608-1135
        • North Florida/South Georgia Veterans Health System, Gainesville, FL
        • 接触:
      • Tampa、Florida、美国、33612
    • New York
      • The Bronx、New York、美国、10468-3904

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  • Veterans eligible for care within the Veterans Health Administration (VHA)
  • Diagnosis of motor incomplete SCI (AIS C-D) for >24-months involving spinal segment lumbar (L)1 or above from trauma, vascular, or orthopedic pathology
  • Low total testosterone (<300 nanograms/decilliter [ng/dL]) and/or low free testosterone (<4.6 ng/dL)
  • Presence of one or more sign of low testosterone, defined as:

    • decreased energy
    • motivation
    • initiative or self-confidence
    • increased fatigue or tiredness
    • reduced sexual desire or activity
    • decreased spontaneous (e.g., morning) erections or erectile dysfunction
    • loss of body hair or reduced shaving
    • feeling sad or blue or having a depressed mood or a persistent low-grade depressive disorder (defined as a score of >3 on the Patient Health Questionnaire [PHQ]-2)
    • hot flashes
    • fatigue or irritability
    • poor concentration or memory
    • mild unexplained (normocytic-normochromic) anemia, defined as hematocrit (HCT) <40%, hemoglobin <13.6 grams/deciliter (g/dL), or red blood cell count <4.5 million/microliter (mcL)
    • sleep disturbances or increased sleepiness
    • reduced muscle bulk, strength, or physical function
    • increased body fat or body mass index
  • Presence of motor impairment, defined as self-selected walking pace ≤1.0 meters/second (m/s) on a 10-meter walk test (10mWT), with or without gait devices or braces and with or without assistance from another person, or as self-selected walking pace >1.0 m/s with reliance on a gait device or brace or with highly compensated movement impairment identified by a trained observer
  • Medically stable condition asymptomatic for bladder infection, major decubiti, cardiopulmonary disease, or other significant condition that will interfere with the study
  • Documented approval from a physician verifying medical status

Exclusion Criteria:

  • Involvement in another research study that may influence outcomes
  • Mental state that precludes understanding the protocol
  • Life expectancy <12 months
  • History of or current congenital spinal cord injury (SCI) (e.g., Chiari malformation, myelomeningocele, intraspinal neoplasm, Friedreich's ataxia) or degenerative spinal disorder (e.g., spinocerebellar degeneration) that may complicate procedures
  • Amyotrophic lateral sclerosis, multiple sclerosis, or other neurologic injury / impairment that may complicate procedures
  • Current cancer diagnosis
  • History of prostate or breast cancer
  • Any diagnosed or treated cancer in the past 24 months, except basal or squamous cell carcinoma of the skin that has been successfully treated
  • Any major lower-limb fracture in the past 12 months
  • Unevaluated circulating prostate-specific antigen (PSA) >4.0 nanograms/milliliter (ng/mL) or >3.0 ng/mL in men with prostate cancer risk factors, including agent orange exposure, first degree relative with prostate cancer, or African American background
  • Currently seeking fertility or expected during the study
  • Diagnosed gynecomastia
  • Hematocrit (HCT) >48%
  • Any major cardiovascular event in the last 6 months, defined as:

    • an acute myocardial infarction
    • any cardiac revascularization procedure including stenting
    • angioplasty or coronary artery bypass grafting
    • revascularization of the carotid or middle cerebral artery or procedure to treat critical limb ischemia
    • hospitalization due to unstable angina
    • transient ischemic attack
    • stroke
    • peripheral vascular disease
  • Any angina that is not controlled on a current medical regimen (Canadian class II, III, or IV)
  • Poorly compensated congestive heart failure (New York Heart Association [NYHA] class III or IV)
  • Poorly controlled hypertension when on medication (consistent systolic BP ≥160 mmHg or diastolic BP ≥100 mmHg)
  • Poorly controlled arrhythmia of any type
  • Severe valvular heart disease
  • Baseline electrocardiogram findings such as left bundle branch block or marked abnormality that precludes serial screening for occult ischemic events
  • History of unprovoked deep venous thrombosis, unprovoked pulmonary embolism, history of recurrent deep venous thrombosis or known thrombophilia
  • Major non-cardiovascular surgery (e.g., major abdominal or thoracic procedure) within 90 days before screening or a major surgery scheduled at the time of screening
  • Liver enzymes (aspartate aminotransferase [AST] or alanine aminotransferase [ALT]) >1.5 times the normal upper limit
  • Severe or end-stage chronic kidney disease defined as eGFR <30 milliliters/minute (mL/min)
  • Diagnosed, but untreated severe obstructive sleep apnea
  • Use of an agent that alters sex-steroid metabolism in the past 90 days, such as: testosterone therapy (TRT), compounded or over-the-counter androgenic hormone or androgen precursor, 5-alpha reductase (5AR) inhibitors, growth hormone, clomiphene, aromatase inhibitors, anti-estrogen or estrogen treatment, or others
  • Use of anti-resorptive or bone anabolic drug therapy in the past 180 days
  • Acute use (>5 days) of any opioid (e.g., oxycodone, hydrocodone) or systemic glucocorticoids >7.5 milligrams (mg)/day prednisone equivalent (e.g., hydrocortisone 30 mg, methylprednisolone 6 mg, or dexamethasone 1.2 mg) in the week before screening, except for men who are taking these for a chronic condition and who are anticipated to continue these for the study duration
  • Known allergy to any TRT component (e.g., cottonseed oil or other)
  • Any other condition, lab abnormality, therapy, medical or psychiatric condition, or reason that might pose a risk to the participant, make participation not in the person's best interest, confound the study results (e.g., inability to comply with study requirements), make the participant unsuitable to receive a study intervention, or interfere with their ability to participate for the full study duration

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:支持治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:四人间

武器和干预

参与者组/臂
干预/治疗
实验性的:testosterone, placebo
Testosterone by intramuscular injection (200 mg/q2wk) and placebo pill orally (5 mg/day)
Participants receive testosterone (200 mg/q2wk) by intramuscular injection
其他名称:
  • depo-testosterone
Participants receive placebo pill (daily) orally
其他名称:
  • 非活性物质
实验性的:testosterone, finasteride
Testosterone by intramuscular injection (200 mg/q2wk) and a finasteride pill orally (5 mg/day)
Participants receive testosterone (200 mg/q2wk) by intramuscular injection
其他名称:
  • depo-testosterone
Participants receive finasteride (5 mg/day) orally
其他名称:
  • 保列治
安慰剂比较:placebo treatment
Placebo by intramuscular injection (q2wk) and a placebo pill orally (daily)
Participants receive placebo pill (daily) orally
其他名称:
  • 非活性物质
Participants receive placebo (weekly) by intramuscular injection
其他名称:
  • 非活性物质

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Change in lower limb fat-free mass
大体时间:Baseline, 9 months
Change from baseline in lower limb fat-free mass assessed via dual-energy X-ray absorptiometry (DXA)
Baseline, 9 months

次要结果测量

结果测量
措施说明
大体时间
Change in total body fat-free mass
大体时间:Baseline, 9 months
Change from baseline in total body fat-free mass assessed via dual-energy X-ray absorptiometry (DXA)
Baseline, 9 months
Change in knee extensor strength
大体时间:Baseline, 9 months
Change from baseline in thigh (knee extensors) peak isometric torque production of the non-dominant limb assessed via dynamometry
Baseline, 9 months
Change in distal femur bone mineral density
大体时间:Baseline, 9 months
Change from baseline in distal femur areal bone mineral density of the non-dominant limb assessed via dual-energy X-ray absorptiometry
Baseline, 9 months
Change in visceral adipose tissue (fat) mass
大体时间:Baseline, 9 months
Change from baseline in visceral adipose tissue (fat) mass assessed via dual-energy X-ray absorptiometry
Baseline, 9 months
Change in prostate specific antigen (PSA)
大体时间:Baseline, 3 months, 6 months, 9 months
Change from baseline n prostate specific antigen (PSA) assessed in the circulation
Baseline, 3 months, 6 months, 9 months

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2027年10月1日

初级完成 (估计的)

2031年9月30日

研究完成 (估计的)

2032年3月31日

研究注册日期

首次提交

2026年7月28日

首先提交符合 QC 标准的

2026年7月28日

首次发布 (实际的)

2026年8月3日

研究记录更新

最后更新发布 (实际的)

2026年8月4日

上次提交的符合 QC 标准的更新

2026年8月3日

最后验证

2026年7月1日

更多信息

与本研究相关的术语

其他研究编号

  • RRDA-011-25W
  • 1I01RD002003-01A1 (其他赠款/资助编号:US Department of Veterans Affairs)

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

是的

IPD 计划说明

Data will be shared according to the requirements described by the Department of Veterans Affairs, Office of Research & Development.

IPD 共享时间框架

Data will be shared according to the requirements described by the Department of Veterans Affairs, Office of Research & Development.

IPD 共享访问标准

Data will be shared according to the requirements described by the Department of Veterans Affairs, Office of Research & Development.

IPD 共享支持信息类型

  • 研究方案
  • 树液
  • 国际碳纤维联合会
  • 分析代码
  • 企业社会责任

药物和器械信息、研究文件

研究美国 FDA 监管的药品

是的

研究美国 FDA 监管的设备产品

不

在美国制造并从美国出口的产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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