Cette page a été traduite automatiquement et l'exactitude de la traduction n'est pas garantie. Veuillez vous référer au version anglaise pour un texte source.

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

Aperçu de l'étude

Type d'étude

Interventionnel

Inscription (Estimé)

100

Phase

  • Phase 4

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Non

La description

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

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Comparateur actif: 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.
Autres noms:
  • Gabapentine
  • Oxybutynine
  • Fezolinetant
  • Selective serotonin reuptake inhibitor (SSRI)
Expérimental: 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

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

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Recruitment Rate
Délai: At enrollment
Proportion of eligible women approached who consent to randomization, Percentage (%)
At enrollment
12-Month Retention Rate
Délai: 12 months
Proportion of randomized participants completing the 12-month follow-up visit, Percentage (%)
12 months
CMR Completion Rate
Délai: 12 months
Proportion of participants completing both baseline and 12-month CMR examinations, Percentage (%)
12 months
Crossover Rate
Délai: 12 months
Proportion of participants in the no-MHT group who initiate systemic MHT during follow-up, Percentage (%)
12 months

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Myocardial oxygenation reserve
Délai: 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
Délai: Baseline and 12 months
assessed by CMR, mmHg-¹
Baseline and 12 months
Aortic cross-sectional area
Délai: Baseline and 12 months
assessed by CMR, cm²
Baseline and 12 months
Left ventricular ejection fraction (LVEF)
Délai: Baseline and 12 months
Assessed by CMR, Percentage (%)
Baseline and 12 months
Left ventricular end-diastolic volume (LVEDV)
Délai: Baseline and 12 months
Assessed by CMR, mL
Baseline and 12 months
Left ventricular end-systolic volume (LVESV)
Délai: Baseline and 12 months
Assessed by CMR, mL
Baseline and 12 months
Left ventricular mass (LVM)
Délai: Baseline and 12 months
Assessed by CMR, grams (g)
Baseline and 12 months
LV mass-to-volume ratio (concentricity)
Délai: Baseline and 12 months
Assessed by CMR, g/mL
Baseline and 12 months
Global longitudinal strain (GLS)
Délai: Baseline and 12 months
Assessed by CMR, Percentage (%)
Baseline and 12 months
Superficial retinal capillary plexus vessel density
Délai: Baseline and 12 months
Assessed by OCT-A, Percentage (%)
Baseline and 12 months
Deep retinal capillary plexus vessel density
Délai: Baseline and 12 months
Assessed by OCT-A, Percentage (%)
Baseline and 12 months
Foveal avascular zone (FAZ) area
Délai: Baseline and 12 months
Assessed by OCT-A, mm2
Baseline and 12 months
FAZ perimeter
Délai: Baseline and 12 months
Assessed by OCT-A, mm
Baseline and 12 months
PROMIS Cognitive Function Short Form 8a score
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

1 novembre 2026

Achèvement primaire (Estimé)

1 novembre 2028

Achèvement de l'étude (Estimé)

1 janvier 2029

Dates d'inscription aux études

Première soumission

25 juin 2026

Première soumission répondant aux critères de contrôle qualité

23 juillet 2026

Première publication (Réel)

29 juillet 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

29 juillet 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

23 juillet 2026

Dernière vérification

1 juillet 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

produit fabriqué et exporté des États-Unis.

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

S'abonner