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Hormone thERapy Effects on BRAin-HEART Health During the Menopausal Transition (HERBRAVEHEART)

HER BRAVE HEART Trial - Hormone thERapy Effects on BRAin-HEART Health During the Menopausal Transition: A Randomized Feasibility Study

The goal of this clinical trial is to learn whether it is feasible to conduct a larger study comparing transdermal menopausal hormone therapy (MHT) versus no hormone therapy in menopausal women with vasomotor symptoms (hot flashes and night sweats) and at least one cardiovascular risk factor. The main questions it aims to answer are:

  • What proportion of eligible women agree to be randomly assigned to either receive MHT or not?
  • How many participants complete the 12-month follow-up, including repeat heart imaging?
  • Does transdermal MHT affect early changes in heart muscle tissue as measured by cardiac MRI?

Researchers will compare immediate initiation of transdermal estradiol (a skin gel or patch) to a no-hormone therapy strategy to see if MHT influences early cardiovascular and brain-vascular changes over 12 months.

Participants will:

  • Be randomly assigned to start transdermal MHT within 2 weeks, or to use no hormone therapy for at least the first 3 months
  • Undergo a cardiac MRI and retinal eye imaging at the start of the study and again at 12 months
  • Complete cognitive testing and questionnaires about symptoms, sleep, and stress at both visits
  • Provide a blood sample for storage and future analysis of heart and brain health markers
  • Receive follow-up phone calls at 3, 6, and 9 months to review symptoms, medications, and any health changes

Visão geral do estudo

Status

Ainda não está recrutando

Condições

Intervenção / Tratamento

Tipo de estudo

Intervencional

Inscrição (Estimado)

100

Estágio

  • Fase 4

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Descrição

Inclusion Criteria:

  • Women aged ≥ 45 years.
  • Perimenopausal or postmenopausal, defined as at least one of the following:

    • Perimenopause, defined as menstrual cycle irregularity (changes in cycle length, skipped cycles, or amenorrhea ≥ 60 days) accompanied by vasomotor symptoms consistent with the menopausal transition.
    • Postmenopause, defined as at least one of:

      • ≥ 12 months of spontaneous amenorrhea, or
      • bilateral oophorectomy, or
      • hysterectomy with FSH > 40 IU/L when menstrual history is unavailable.
  • Vasomotor symptoms with a negative impact on quality of life, defined as :

    • Recurrent hot flashes (sudden sensations of heat, typically involving the face, neck, or chest, often associated with flushing and/or sweating), and/or
    • Night sweats (episodes of excessive sweating during sleep), With associated interference in daily functioning, sleep, or overall quality of life, such that the participant would be an appropriate candidate for systemic menopausal hormone therapy in clinical practice.
  • Presence of at least one cardiovascular risk factor, defined as either:

    • Hypertension (diagnosed hypertension, use of antihypertensive medication, or blood pressure ≥ 140/90 mmHg on screening).
    • Dyslipidemia (diagnosed dyslipidemia, use of lipid-lowering therapy, LDL ≥ 3.0 mmol/L, or total cholesterol ≥ 5.2 mmol/L).
    • Type 2 diabetes mellitus, defined as HbA1c ≥ 6.5%, fasting plasma glucose ≥ 7.0 mmol/L, or use of glucose-lowering medication.
    • Obesity (body mass index ≥ 30 kg/m²).
    • Current smoking.
    • First-degree family history of premature cardiovascular disease, defined as myocardial infarction, stroke, or documented coronary artery disease occurring before age 55 years in a male relative or before age 65 years in a female relative.
  • Eligible for systemic MHT (i.e., no formal contraindication to MHT).
  • Able and willing to undergo research CMR and attend the 12-month follow-up assessment.
  • Able to provide written informed consent.
  • Not currently using systemic MHT at baseline, or willing to discontinue systemic MHT prior to randomization and remain off systemic MHT until allocation and baseline assessments are complete.

Exclusion Criteria:

  • Prior cardiovascular event or established cardiovascular disease, including myocardial infarction, stroke or TIA, coronary artery disease, heart failure, cardiomyopathy, or clinically significant valvular heart disease.
  • Uncontrolled hypertension or other unstable cardiovascular condition (e.g., unstable angina, decompensated heart failure, uncontrolled arrhythmia).
  • Formal contraindication to systemic menopausal hormone therapy, including estrogen-dependent cancer, unexplained vaginal bleeding, active severe liver disease, severe thrombophilia, antiphospholipid syndrome, prior or active VTE.
  • Standard contraindications to MRI (e.g., MRI-incompatible pacemakers or intracardiac devices, certain metallic implants, metallic foreign bodies in the eye, or severe claustrophobia not manageable).
  • Pregnant.
  • Active cancer on ongoing cardiotoxic chemotherapy.
  • Current use of systemic hormonal therapy outside the study strategy, including systemic menopausal hormone therapy, combined hormonal contraception, or systemic progestin-only contraception, with unwillingness or inability to discontinue prior to baseline and randomization.
  • Ten years or more since menopause, defined as ≥10 years from the final menstrual period or from bilateral oophorectomy
  • Participants currently using combined hormonal contraception or systemic progestin-only contraception who are willing to discontinue must complete a washout period of at least 4 weeks prior to the baseline visit and randomization

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Comparador Ativo: Non Hormonal Management of Vasomotor Symptoms
Non hormonal management of vasomotor symptoms
Participants randomized to this arm will not initiate systemic menopausal hormone therapy for at least the first 3 months following randomization. Non-hormonal management of vasomotor symptoms is permitted at the discretion of the treating physician, and may include lifestyle interventions, supplements, and/or guideline-recommended non-hormonal pharmacologic therapies such as SSRIs/SNRIs, gabapentin, oxybutynin, or fezolinetant. If participants experience persistent or intolerable vasomotor symptoms despite non-hormonal management, initiation of systemic MHT may be proposed after 3 months based on shared decision-making between the participant and her treating physician. All crossovers will be documented including timing, reason, and regimen. Participants will remain analyzed in their originally assigned group for intention-to-treat analyses.
Outros nomes:
  • Gabapentina
  • Oxibutinina
  • Fezolinetant
  • Selective serotonin reuptake inhibitor (SSRI)
Experimental: Transdermal Menopausal Hormone Therapy

Participants randomized to this arm will initiate systemic transdermal estradiol within 2 weeks of the baseline visit. The specific formulation and dose will be selected through shared decision-making between the participant and her physician based on individual clinical factors, tolerability, and patient preference. Permitted formulations include:

Estrogel® (0.06% estradiol gel): 1 pump (0.75 mg) to 2 pumps (1.5 mg) applied daily Divigel® (0.1% estradiol gel): 1.0 mg sachet applied once daily Estradot® (estradiol patch): 25, 37.5, or 50 mcg, changed twice weekly Climara® (estradiol patch): 25, 37.5, or 50 mcg, changed once weekly Participants with a uterus will receive endometrial protection. First-line therapy is micronized progesterone (Prometrium® 100 mg orally once daily, continuous regimen). Alternative progestogens (medroxyprogesterone acetate 2.5 mg orally once daily or a levonorgestrel-releasing intrauterine device) may be used if clinically indicated or not tolerated. Dose ad

Outros nomes:
  • Estrogel® (estradiol 0.06% gel)
  • Divigel® (estradiol 0.1% gel)
  • Estradot® (estradiol transdermal patch)
  • Climara® (estradiol transdermal patch)

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Recruitment Rate
Prazo: At enrollment
Proportion of eligible women approached who consent to randomization, Percentage (%)
At enrollment
12-Month Retention Rate
Prazo: 12 months
Proportion of randomized participants completing the 12-month follow-up visit, Percentage (%)
12 months
CMR Completion Rate
Prazo: 12 months
Proportion of participants completing both baseline and 12-month CMR examinations, Percentage (%)
12 months
Crossover Rate
Prazo: 12 months
Proportion of participants in the no-MHT group who initiate systemic MHT during follow-up, Percentage (%)
12 months

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Myocardial oxygenation reserve
Prazo: Baseline and 12 months
Percent change in myocardial signal intensity (ΔSI%) during breath-hold at 30 seconds relative to rest, assessed by OS-CMR (B-MORE)
Baseline and 12 months
Aortic distensibility
Prazo: Baseline and 12 months
assessed by CMR, mmHg-¹
Baseline and 12 months
Aortic cross-sectional area
Prazo: Baseline and 12 months
assessed by CMR, cm²
Baseline and 12 months
Left ventricular ejection fraction (LVEF)
Prazo: Baseline and 12 months
Assessed by CMR, Percentage (%)
Baseline and 12 months
Left ventricular end-diastolic volume (LVEDV)
Prazo: Baseline and 12 months
Assessed by CMR, mL
Baseline and 12 months
Left ventricular end-systolic volume (LVESV)
Prazo: Baseline and 12 months
Assessed by CMR, mL
Baseline and 12 months
Left ventricular mass (LVM)
Prazo: Baseline and 12 months
Assessed by CMR, grams (g)
Baseline and 12 months
LV mass-to-volume ratio (concentricity)
Prazo: Baseline and 12 months
Assessed by CMR, g/mL
Baseline and 12 months
Global longitudinal strain (GLS)
Prazo: Baseline and 12 months
Assessed by CMR, Percentage (%)
Baseline and 12 months
Superficial retinal capillary plexus vessel density
Prazo: Baseline and 12 months
Assessed by OCT-A, Percentage (%)
Baseline and 12 months
Deep retinal capillary plexus vessel density
Prazo: Baseline and 12 months
Assessed by OCT-A, Percentage (%)
Baseline and 12 months
Foveal avascular zone (FAZ) area
Prazo: Baseline and 12 months
Assessed by OCT-A, mm2
Baseline and 12 months
FAZ perimeter
Prazo: Baseline and 12 months
Assessed by OCT-A, mm
Baseline and 12 months
PROMIS Cognitive Function Short Form 8a score
Prazo: Baseline and 12 months
Patient-reported cognitive function; scores range 8-40, higher scores indicate better cognitive function
Baseline and 12 months
RBANS Total Scale Score
Prazo: Baseline and 12 months
Objective neuropsychological assessment of global cognitive function; standardized score (mean 100, SD 15), higher scores indicate better performance
Baseline and 12 months
Global native myocardial T1 according to vasomotor symptom burden
Prazo: Baseline
Baseline native T1 (ms) assessed by CMR, compared between women with high vs. low vasomotor symptom burden at baseline, defined by HFRDIS score
Baseline
LVEF according to vasomotor symptom burden
Prazo: Baseline
Baseline LVEF assessed by CMR, compared between women with high vs. low vasomotor symptom burden at baseline, defined by HFRDIS score, Percentage (%)
Baseline
Multivariable regression analysis of baseline predictors of 12-month change in global native myocardial T1
Prazo: Baseline and 12 months
Exploratory multivariable linear regression will be used to identify associations between baseline clinical, lifestyle, and menopause-related factors (including age, BMI, blood pressure, lipid levels, smoking status, time since menopause, and vasomotor symptom burden) and 12-month change in global native myocardial T1 assessed by CMR. This analysis aims to identify candidate predictors for future cardiovascular risk stratification. The dependent variable is change in global native T1 (ms) from baseline to 12 months.
Baseline and 12 months

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Patrocinador

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

1 de novembro de 2026

Conclusão Primária (Estimado)

1 de novembro de 2028

Conclusão do estudo (Estimado)

1 de janeiro de 2029

Datas de inscrição no estudo

Enviado pela primeira vez

25 de junho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

23 de julho de 2026

Primeira postagem (Real)

29 de julho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

29 de julho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

23 de julho de 2026

Última verificação

1 de julho de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

produto fabricado e exportado dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .