- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07742553
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
Aperçu de l'étude
Statut
Les conditions
- Maladies du système nerveux
- Blessures et Blessures
- Maladies du système endocrinien
- Troubles gonadiques
- Traumatisme, système nerveux
- Maladies de la moelle épinière
- Hypogonadisme
- Blessures à la moelle épinière
- Lésion de la moelle épinière
- Compression de la moelle épinière
- Maladies génitales, sexe masculin
- Contusion de la moelle épinière
- Traumatisme de la moelle épinière
- Blessures, moelle épinière
Intervention / Traitement
Description détaillée
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.
Type d'étude
Inscription (Estimé)
Phase
- Phase 2
- Phase 3
Contacts et emplacements
Coordonnées de l'étude
- Nom: Joshua F Yarrow, PhD MS BS
- Numéro de téléphone: (720) 857-5520
- E-mail: joshua.yarrow@va.gov
Lieux d'étude
-
-
Colorado
-
Aurora, Colorado, États-Unis, 80045-7211
- Rocky Mountain Regional VA Medical Center, Aurora, CO
-
Contact:
- Joshua F Yarrow, PhD MS BS
- Numéro de téléphone: (720) 857-5520
- E-mail: joshua.yarrow@va.gov
-
Chercheur principal:
- Joshua F Yarrow, PhD MS BS
-
-
Florida
-
Gainesville, Florida, États-Unis, 32608-1135
- North Florida/South Georgia Veterans Health System, Gainesville, FL
-
Contact:
- Dana Otzel, PhD
- E-mail: Dana.Otzel@va.gov
-
Tampa, Florida, États-Unis, 33612
- James A. Haley Veterans' Hospital, Tampa, FL
-
Contact:
- Kevin White, MD
- E-mail: Kevin.White2@va.gov
-
Contact:
- Brittany Durant, RN
- E-mail: Brittany.Durant@va.gov
-
-
New York
-
The Bronx, New York, États-Unis, 10468-3904
- James J. Peters VA Medical Center, Bronx, NY
-
Contact:
- Christopher Cardozo, MD
- E-mail: Christopher.Cardozo@va.gov
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
La description
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 d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Soins de soutien
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Quadruple
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: 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
Autres noms:
Participants receive placebo pill (daily) orally
Autres noms:
|
|
Expérimental: 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
Autres noms:
Participants receive finasteride (5 mg/day) orally
Autres noms:
|
|
Comparateur placebo: placebo treatment
Placebo by intramuscular injection (q2wk) and a placebo pill orally (daily)
|
Participants receive placebo pill (daily) orally
Autres noms:
Participants receive placebo (weekly) by intramuscular injection
Autres noms:
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Change in lower limb fat-free mass
Délai: Baseline, 9 months
|
Change from baseline in lower limb fat-free mass assessed via dual-energy X-ray absorptiometry (DXA)
|
Baseline, 9 months
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Change in total body fat-free mass
Délai: 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
Délai: 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
Délai: 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
Délai: 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)
Délai: 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
|
Collaborateurs et enquêteurs
Parrainer
Collaborateurs
Les enquêteurs
- Chercheur principal: Joshua F Yarrow, PhD MS BS, Rocky Mountain Regional VA Medical Center, Aurora, CO
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
- Démarche
- Maladies du système nerveux
- La composition corporelle
- Maladies du système nerveux central
- Maladies musculo-squelettiques
- En marchant
- Lésion de la moelle épinière
- Hypogonadisme
- Force musculaire
- Activité motrice
- Maladies osseuses
- Actions pharmacologiques
- Locomotion
- Stéroïdes
- Utilisations thérapeutiques
- Maladies du système endocrinien
- Testostérone
- Maladies de la moelle épinière
- Blessures et Blessures
- Agents de conservation de la densité osseuse
- Masse musculaire
- Androgènes
- Les hormones
- Formation osseuse
- Finastéride
- Tissu adipeux
- Os et os
- Blessures à la moelle épinière
- Densité minérale osseuse
- Graisse corporelle
- Maladies urogénitales masculines
- Maladies génitales, sexe masculin
- Énanthate de testostérone
- Dihydrotestostérone
- Troubles gonadiques
- Undécanoate de testostérone
- Testostérone 17 bêta-cypionate
- Méthyltestostérone
- Substituts hormonaux et antagonistes hormonaux
- Effets physiologiques des médicaments
- Agents anabolisants
- Thérapie de remplacement de la testostérone
- Absorptiométrie double énergie à rayons X
- Masse tissulaire maigre
- Densité, Os
- La résorption osseuse
- Thérapie à la testostérone
- 5-alpha réductase
- Profil lipidique et glycémique
- Muscle, Squelette
- Maladies génitales
- Masse grasse
- Traumatisme, système nerveux
- Cypionate de testostérone
- Maladies urogénitales
- Testosterone propionate
Termes MeSH pertinents supplémentaires
- Comportement
- Maladies urogénitales
- Maladies génitales
- Blessures et Blessures
- Hypogonadisme
- Blessures à la moelle épinière
- Maladies musculo-squelettiques
- La résorption osseuse
- Maladies du système nerveux
- Maladies du système nerveux central
- Maladies osseuses
- Maladies du système endocrinien
- Maladies urogénitales masculines
- Maladies de la moelle épinière
- Compression de la moelle épinière
- Traumatisme, système nerveux
- Maladies génitales, sexe masculin
- Troubles gonadiques
- Activité motrice
- Composés polycycliques
- Stéroïdes
- Composés à anneau fusionné
- Androsténes
- Androstanes
- Azasteroïds
- Stéroïdes, hétérocyclique
- Finastéride
- testostérone 17 bêta-cypionate
Autres numéros d'identification d'étude
- RRDA-011-25W
- 1I01RD002003-01A1 (Autre subvention/numéro de financement: US Department of Veterans Affairs)
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Description du régime IPD
Délai de partage IPD
Critères d'accès au partage IPD
Type d'informations de prise en charge du partage d'IPD
- PROTOCOLE D'ÉTUDE
- SÈVE
- CIF
- ANALYTIC_CODE
- RSE
Informations sur les médicaments et les dispositifs, documents d'étude
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