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- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT04922424
Mechanisms and Interventions to Address Cardiovascular Risk of Gender-affirming Hormone Therapy in Trans Men
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
Tipo de estudio
Fase
- Fase 1
Contactos y Ubicaciones
Ubicaciones de estudio
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Connecticut
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New Haven, Connecticut, Estados Unidos, 06519
- Yale School of Medicine
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Two groups (n=10 each) of subjects will be recruited to complete this study: 1) trans men between 18 and 35 years; 2) cisgender women between 18 and 35 years (Controls). They will have a body mass index (BMI) 18-30 kg·m-2. Our subjects will be matched on BMI and IR, using hemoglobin A1c and Homeostatic Model Assessment of Insulin Resistance technique (HOMA-IR) in order to isolate testosterone effects from other co-morbidities that may impact BP, sympathetic activity or endothelial function. Subjects will have HbA1c of 4-5.9% and a HOMA-IR of 0.5-1.4 to be included in the study. Subjects who smoke, have diabetes, or BP>140/90 will be excluded. Subjects will not be taking medications during the study, including any insulin sensitizing or CV medications.
Exclusion Criteria:
- Subjects with the following histories or conditions will be excluded from the study:
Gynecologic: a. current or past estrogen-dependent neoplasia, b. unexplained vaginal bleeding, c. history of uterine fibroids, d. current pregnancy, e. known or suspected breast or uterine cancer, f. partial or complete hysterectomy.
Cardiac: a. myocardial infarction, ventricular tachycardia or fibrillation, b. angina, c. valvular disease (mitral insufficiency or stenosis, aortic insufficiency or stenosis), d. congestive heart failure, orthopnea, paroxysmal nocturnal dyspnea, e. current arrhythmias, f. prosthetic valves.
Pulmonary: a. current cigarette smokers, or pipe or cigar smokers, b. chronic obstructive pulmonary disease, c. adult asthma, d. dyspnea on exertion, e. current bronchitis, pneumonia, or tuberculosis, f. lung carcinoma, g. pulmonary embolus, h. deep vein thrombosis.
Vascular: a. claudications or history of peripheral vascular disease, b. abdominal or thoracic aortic aneurysm, or repair of same, c. cerebral aneurysm, vascular malformations, d. hypertension, systolic or diastolic, or strong family history of hypertension.
Gastrointestinal: a. GI malignancy, b. hepatitis or other liver disease, current, c. splenomegaly from any cause, d. Cholecystitis, e. current diverticulosis or diverticulitis, inflammatory bowel disease, ulcerative colitis, Crohn's disease, f. previous gastrointestinal surgery.
Infectious Disease: any ongoing intercurrent infection. Hematologic/Oncologic: a. receiving chemotherapy or radiation therapy, b. any metastatic malignancy, c. anemia (hematocrit < 35), d. thrombocytopenia or thrombocytosis, e. neutropenia, f. hematologic malignancy, g. bleeding dyscrasia.
Neurologic: a. history of cerebral vascular accident with any neurologic sequels, b. uncontrolled seizures (e.g., more than 1 seizure/year), c. transient ischemic attacks, d. dementia, e. neurologic conditions producing dyscoordination, peripheral neuropathy, or myopathy.
Endocrine: a. diabetes mellitus, b. any untreated endocrinopathy. Renal: a. chronic renal diseases, b. any history of renal disease or impairment, c. current urinary tract infection.
Musculoskeletal: a. inflammatory arthritis history (e.g., rheumatoid, psoriatic, Reiters), b. any history of pathologic fractures, including vertebral compression fractures.
Pharmacologic: a. any illegal drug use, b. alcohol use greater than an average of 4 oz/day over 30 days, c. coumadin or heparin use.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Otro
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación cruzada
- Enmascaramiento: Triple
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Experimental: atorvastatin
We are testing that the lipid sensitive statin, atorvastatin treatment will reduce low density lipoprotein cholesterone, sympathetic nerve activity, increase endothelium-dependent vasodilation and improve autonomic function in trans men, while having little impact on cis women.
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Subjects will ingest placebo or ingest 20 mg atorvastatin for 30 days first.
We will include 30 days of washout between treatments to minimize any potential carryover effects.
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Comparador de placebos: Placebo
We are testing that the placebo will have little effect on low density lipoprotein cholesterone, sympathetic nerve activity, endothelium-dependent vasodilation, autonomic function in trans men or cis women.
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Subjects will ingest placebo or ingest 20 mg atorvastatin for 30 days first.
We will include 30 days of washout between treatments to minimize any potential
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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flow mediated vasodilation (FMD)
Periodo de tiempo: 30 minutes
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FMD measures endothelial function, measured in % change from baseline arterial diameter after release following a short period of occlusion occlusion.
The % change in diameter reflects the ability of the vessel to dilate in response to sheer stress induced by the flow following the release of occlusion.
This reflects the function of the endothelium, or release of nitric oxide.
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30 minutes
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Muscle Sympathetic Nerve activity (MSNA)
Periodo de tiempo: 2 hours
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measured using microneurography and expressed in bursts/min or bursts/100 heart beats
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2 hours
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Cardiovagal baroreflex sensitivity (BRS)
Periodo de tiempo: 2 hours
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This is determined as a function of change in R-R interval (from EKG) over systolic blood pressure during rest and regular breathing.
Expressed in Units.
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2 hours
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Mental Stress Test
Periodo de tiempo: 10 minutes
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While measuring sympathetic nervous system activity (SNS) with microneurography, we ask the subject to count backwards from 200 by 7.
This increases SNS.
Measured in bursts/min or burst/100 heart beats
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10 minutes
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Voluntary Breath-Hold
Periodo de tiempo: 10 minutes
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While measuring sympathetic nervous system activity (SNS) with microneurography, we ask the subject to hold breath as long as possible without straining.
The subject does this twice, with a break in between.
This increases SNS.
Measured in bursts/min or burst/100 heart beats
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10 minutes
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Systolic Blood Pressure
Periodo de tiempo: 2 hours
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SBP, measured in mmHg
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2 hours
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Diastolic Blood Pressure
Periodo de tiempo: 2 hours
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DBP, measured in mmHg
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2 hours
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serum total cholesterol
Periodo de tiempo: 5 minutes
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Measured in ng/dl.
Elevated total cholesterol can indicate dyslipidemia.
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5 minutes
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serum low density lipoprotein (LDL)-C
Periodo de tiempo: 5 minutes
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Measured in ng/dl.
Elevated LDL-C can indicate dyslipidemia
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5 minutes
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serum high density lipoprotein (HDL-C)
Periodo de tiempo: 5 minutes
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Measured in ng/dl.
Low HDL-C can indicate dyslipidemia
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5 minutes
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plasma endothelin-1, (S[ET-1])
Periodo de tiempo: 5 minutes
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endothelial health, increased ET-1 levels in the blood indicate damage to the endothelium
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5 minutes
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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plasma Catecholamines
Periodo de tiempo: 5 minutes
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Measure of norepinephrine in pg/ml is a measure of whole body sympathetic nervous system outflow
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5 minutes
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serum estradiol (S[E2])
Periodo de tiempo: 5 minutes
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estrogen is measured in pg/ml.
This should be suppressed in our trans subjects, and low in our cis subjects.
In the latter, low estrogen should indicate the early follicular phase of the menstrual cycle.
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5 minutes
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serum progesterone (S[P4])
Periodo de tiempo: 5 minutes
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progesterone is measured in pg/ml.
This should be suppressed in our trans subjects, and low in our cis subjects.
In the latter, low progesterone should indicate the early follicular or ovulatory phases of the menstrual cycle.
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5 minutes
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serum sex hormone binding globulin (P[SHBG])
Periodo de tiempo: 5 minutes
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measured in pg/ml.
This provides us with an indication of how much testosterone is free versus bound in the serum, and thus is available for biological function.
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5 minutes
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serum testosterone
Periodo de tiempo: 5 minutes
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measured in pg/ml.
This indicates the level of testosterone in our trans men showing they are receiving treatment.
It should be high in our trans men and low in our cis women subjects.
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5 minutes
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plasma creatinine
Periodo de tiempo: 5 minutes
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This is a measure of kidney function.
Important for blood pressure regulation
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5 minutes
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Nina Stachenfeld, Yale School of Medicine
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Anticipado)
Finalización primaria (Anticipado)
Finalización del estudio (Anticipado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
- Enfermedades metabólicas
- Trastornos del metabolismo de los lípidos
- Dislipidemias
- Hiperlipidemias
- Mecanismos moleculares de acción farmacológica
- Inhibidores de enzimas
- Antimetabolitos
- Agentes Anticolesterolémicos
- Agentes hipolipidémicos
- Agentes reguladores de lípidos
- Inhibidores de la hidroximetilglutaril-CoA reductasa
- Atorvastatina
Otros números de identificación del estudio
- 2000030176
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
producto fabricado y exportado desde los EE. UU.
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