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

3 de agosto de 2026 actualizado por: 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.

Descripción general del estudio

Descripción detallada

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.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

300

Fase

  • Fase 2
  • Fase 3

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

  • Nombre: Joshua F Yarrow, PhD MS BS
  • Número de teléfono: (720) 857-5520
  • Correo electrónico: joshua.yarrow@va.gov

Ubicaciones de estudio

    • Colorado
      • Aurora, Colorado, Estados Unidos, 80045-7211
        • Rocky Mountain Regional VA Medical Center, Aurora, CO
        • Contacto:
          • Joshua F Yarrow, PhD MS BS
          • Número de teléfono: (720) 857-5520
          • Correo electrónico: joshua.yarrow@va.gov
        • Investigador principal:
          • Joshua F Yarrow, PhD MS BS
    • Florida
      • Gainesville, Florida, Estados Unidos, 32608-1135
        • North Florida/South Georgia Veterans Health System, Gainesville, FL
        • Contacto:
      • Tampa, Florida, Estados Unidos, 33612
    • New York
      • The Bronx, New York, Estados Unidos, 10468-3904

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Descripción

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

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Cuidados de apoyo
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Cuadruplicar

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: 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
Otros nombres:
  • depo-testosterone
Participants receive placebo pill (daily) orally
Otros nombres:
  • sustancia inactiva
Experimental: 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
Otros nombres:
  • depo-testosterone
Participants receive finasteride (5 mg/day) orally
Otros nombres:
  • proscar
Comparador de placebos: placebo treatment
Placebo by intramuscular injection (q2wk) and a placebo pill orally (daily)
Participants receive placebo pill (daily) orally
Otros nombres:
  • sustancia inactiva
Participants receive placebo (weekly) by intramuscular injection
Otros nombres:
  • sustancia inactiva

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in lower limb fat-free mass
Periodo de tiempo: Baseline, 9 months
Change from baseline in lower limb fat-free mass assessed via dual-energy X-ray absorptiometry (DXA)
Baseline, 9 months

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in total body fat-free mass
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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)
Periodo de tiempo: 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

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

1 de octubre de 2027

Finalización primaria (Estimado)

30 de septiembre de 2031

Finalización del estudio (Estimado)

31 de marzo de 2032

Fechas de registro del estudio

Enviado por primera vez

28 de julio de 2026

Primero enviado que cumplió con los criterios de control de calidad

28 de julio de 2026

Publicado por primera vez (Actual)

3 de agosto de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

4 de agosto de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

3 de agosto de 2026

Última verificación

1 de julio de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • RRDA-011-25W
  • 1I01RD002003-01A1 (Otro número de subvención/financiamiento: US Department of Veterans Affairs)

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

SÍ

Descripción del plan IPD

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

Marco de tiempo para compartir IPD

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

Criterios de acceso compartido de IPD

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

Tipo de información de apoyo para compartir IPD

  • PROTOCOLO DE ESTUDIO
  • SAVIA
  • CIF
  • CÓDIGO_ANALÍTICO
  • RSC

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

Sí

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

producto fabricado y exportado desde los EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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