Testosterone Therapy With or Without Finasteride After Spinal Cord Injury: TRT-SCI Trial (TRT-SCI)
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
Studieoversigt
Status
Status
Betingelser
Betingelser
Intervention / Behandling
Intervention / Behandling
Detaljeret 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.
Undersøgelsestype
Undersøgelsestype
Tilmelding (Anslået)
Tilmelding
Fase
Fase
- Fase 2
- Fase 3
Kontakter og lokationer
Studiekontakt
Studiekontakt
- Navn: Joshua F Yarrow, PhD MS BS
- Telefonnummer: (720) 857-5520
- E-mail: joshua.yarrow@va.gov
Studiesteder
-
-
Colorado
-
Aurora, Colorado, Forenede Stater, 80045-7211
- Rocky Mountain Regional VA Medical Center, Aurora, CO
-
Kontakt:
- Joshua F Yarrow, PhD MS BS
- Telefonnummer: (720) 857-5520
- E-mail: joshua.yarrow@va.gov
-
Ledende efterforsker:
- Joshua F Yarrow, PhD MS BS
-
-
Florida
-
Gainesville, Florida, Forenede Stater, 32608-1135
- North Florida/South Georgia Veterans Health System, Gainesville, FL
-
Kontakt:
- Dana Otzel, PhD
- E-mail: Dana.Otzel@va.gov
-
Tampa, Florida, Forenede Stater, 33612
- James A. Haley Veterans' Hospital, Tampa, FL
-
Kontakt:
- Kevin White, MD
- E-mail: Kevin.White2@va.gov
-
Kontakt:
- Brittany Durant, RN
- E-mail: Brittany.Durant@va.gov
-
-
New York
-
The Bronx, New York, Forenede Stater, 10468-3904
- James J. Peters VA Medical Center, Bronx, NY
-
Kontakt:
- Christopher Cardozo, MD
- E-mail: Christopher.Cardozo@va.gov
-
-
Deltagelseskriterier
Berettigelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
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
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Støttende pleje
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Firedobbelt
Antal våben
Våben og indgreb
Deltagergruppe / ArmDeltagergruppe / Arm |
Intervention / BehandlingIntervention / Behandling |
|---|---|
|
Eksperimentel: 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 navne:
Participants receive placebo pill (daily) orally
Andre navne:
|
|
Eksperimentel: 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 navne:
Participants receive finasteride (5 mg/day) orally
Andre navne:
|
|
Placebo komparator: placebo treatment
Placebo by intramuscular injection (q2wk) and a placebo pill orally (daily)
|
Participants receive placebo pill (daily) orally
Andre navne:
Participants receive placebo (weekly) by intramuscular injection
Andre navne:
|
Hvad måler undersøgelsen?
Primære resultatmål
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
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
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
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
|
Samarbejdspartnere og efterforskere
Sponsor
Sponsor
Samarbejdspartnere
Samarbejdspartnere
Efterforskere
Efterforskere
- Ledende efterforsker: Joshua F Yarrow, PhD MS BS, Rocky Mountain Regional VA Medical Center, Aurora, CO
Datoer for undersøgelser
Studer store datoer
Studiestart (Anslået)
Studiestart
Primær færdiggørelse (Anslået)
Primær færdiggørelse
Studieafslutning (Anslået)
Studieafslutning
Datoer for studieregistrering
Først indsendt
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Først opslået
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering sendt
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
- Gang
- Sygdomme i nervesystemet
- Kropssammensætning
- Sygdomme i centralnervesystemet
- Muskuloskeletale sygdomme
- Gåture
- Rygmarvsskade
- Hypogonadisme
- Muskelstyrke
- Motorisk aktivitet
- Knoglesygdomme
- Farmakologiske handlinger
- Bevægelse
- Steroider
- Terapeutiske anvendelser
- Sygdomme i det endokrine system
- Testosteron
- Rygmarvssygdomme
- Sår og skader
- Knogletæthedsbevarende midler
- Muskelmasse
- Androgener
- Hormoner
- Knogledannelse
- Finasteride
- Fedtvæv
- Knogler og Knogler
- Rygmarvsskader
- Knoglemineraltæthed
- Kropsfedt
- Mandlige urogenitale sygdomme
- Kønssygdomme, mandlige
- Testosteron enanthate
- Dihydrotestosteron
- Gonadale lidelser
- Testosteron undecanoat
- Testosteron 17 beta-cypionat
- Methyltestosteron
- Hormonerstatninger og hormonantagonister
- Lægemidlers fysiologiske virkninger
- Anabolske midler
- Testosteron erstatningsterapi
- Dual Energy X-ray Absorptiometri
- Magert vævsmasse
- Tæthed, Knogle
- Knogleresorption
- Testosteron terapi
- 5-alfa-reduktase
- Lipid og Glucose profil
- Muskel, skelet
- Genitale sygdomme
- Fedtmasse
- Traumer, nervesystemet
- Testosteron cypionat
- Urogenitale sygdomme
- Testosterone propionate
Yderligere relevante MeSH-vilkår
- Opførsel
- Urogenitale sygdomme
- Genitale sygdomme
- Sår og skader
- Hypogonadisme
- Rygmarvsskader
- Muskuloskeletale sygdomme
- Knogleresorption
- Sygdomme i nervesystemet
- Sygdomme i centralnervesystemet
- Knoglesygdomme
- Sygdomme i det endokrine system
- Mandlige urogenitale sygdomme
- Rygmarvssygdomme
- Rygmarvskompression
- Traumer, nervesystemet
- Kønssygdomme, mandlige
- Gonadale lidelser
- Motorisk aktivitet
- Polycykliske forbindelser
- Steroider
- SMUSED-RING-forbindelser
- Androstenes
- Androstanes
- Azasteroider
- Steroider, heterocyklisk
- Finasteride
- Testosteron 17 beta-cypionat
Andre undersøgelses-id-numre
Andre undersøgelses-id-numre
- RRDA-011-25W
- 1I01RD002003-01A1 (Andet bevillings-/finansieringsnummer: US Department of Veterans Affairs)
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
IPD-planbeskrivelse
IPD-delingstidsramme
IPD-delingsadgangskriterier
IPD-deling Understøttende informationstype
- STUDY_PROTOCOL
- SAP
- ICF
- ANALYTIC_CODE
- CSR
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
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