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

3. august 2026 oppdatert av: 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.

Studieoversikt

Detaljert beskrivelse

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.

Studietype

Intervensjonell

Registrering (Antatt)

300

Fase

  • Fase 2
  • Fase 3

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studiesteder

    • Colorado
      • Aurora, Colorado, Forente stater, 80045-7211
        • Rocky Mountain Regional VA Medical Center, Aurora, CO
        • Ta kontakt med:
        • Hovedetterforsker:
          • Joshua F Yarrow, PhD MS BS
    • Florida
      • Gainesville, Florida, Forente stater, 32608-1135
        • North Florida/South Georgia Veterans Health System, Gainesville, FL
        • Ta kontakt med:
      • Tampa, Florida, Forente stater, 33612
    • New York
      • The Bronx, New York, Forente stater, 10468-3904

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Nei

Beskrivelse

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

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Støttende omsorg
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Firemannsrom

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: 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
Andre navn:
  • depo-testosterone
Participants receive placebo pill (daily) orally
Andre navn:
  • inaktivt stoff
Eksperimentell: 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
Andre navn:
  • depo-testosterone
Participants receive finasteride (5 mg/day) orally
Andre navn:
  • proscar
Placebo komparator: placebo treatment
Placebo by intramuscular injection (q2wk) and a placebo pill orally (daily)
Participants receive placebo pill (daily) orally
Andre navn:
  • inaktivt stoff
Participants receive placebo (weekly) by intramuscular injection
Andre navn:
  • inaktivt stoff

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Change in lower limb fat-free mass
Tidsramme: Baseline, 9 months
Change from baseline in lower limb fat-free mass assessed via dual-energy X-ray absorptiometry (DXA)
Baseline, 9 months

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Change in total body fat-free mass
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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)
Tidsramme: 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

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

1. oktober 2027

Primær fullføring (Antatt)

30. september 2031

Studiet fullført (Antatt)

31. mars 2032

Datoer for studieregistrering

Først innsendt

28. juli 2026

Først innsendt som oppfylte QC-kriteriene

28. juli 2026

Først lagt ut (Faktiske)

3. august 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

4. august 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

3. august 2026

Sist bekreftet

1. juli 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • RRDA-011-25W
  • 1I01RD002003-01A1 (Annet stipend/finansieringsnummer: US Department of Veterans Affairs)

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

JA

IPD-planbeskrivelse

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

IPD-delingstidsramme

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

Tilgangskriterier for IPD-deling

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

IPD-deling Støtteinformasjonstype

  • STUDY_PROTOCOL
  • SEVJE
  • ICF
  • ANALYTIC_CODE
  • CSR

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Ja

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

produkt produsert i og eksportert fra USA

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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