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
調査の概要
状態
状態
条件
条件
介入・治療
介入・治療
研究の種類
研究の種類
入学 (推定)
入学
段階
段階
- フェーズ 4
連絡先と場所
研究連絡先
研究連絡先
- 名前:Amytis HEIM, MD
- 電話番号:12633813556
- メール:amytis.heim@mail.mcgill.ca
参加基準
適格基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
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
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:なし(オープンラベル)
アーム数
武器と介入
参加者グループ / アーム参加者グループ / アーム |
介入・治療介入・治療 |
|---|---|
|
アクティブコンパレータ: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.
他の名前:
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実験的: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
他の名前:
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この研究は何を測定していますか?
主要な結果の測定
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Recruitment Rate
時間枠:At enrollment
|
Proportion of eligible women approached who consent to randomization, Percentage (%)
|
At enrollment
|
|
12-Month Retention Rate
時間枠:12 months
|
Proportion of randomized participants completing the 12-month follow-up visit, Percentage (%)
|
12 months
|
|
CMR Completion Rate
時間枠:12 months
|
Proportion of participants completing both baseline and 12-month CMR examinations, Percentage (%)
|
12 months
|
|
Crossover Rate
時間枠:12 months
|
Proportion of participants in the no-MHT group who initiate systemic MHT during follow-up, Percentage (%)
|
12 months
|
二次結果の測定
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Myocardial oxygenation reserve
時間枠: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
時間枠:Baseline and 12 months
|
assessed by CMR, mmHg-¹
|
Baseline and 12 months
|
|
Aortic cross-sectional area
時間枠:Baseline and 12 months
|
assessed by CMR, cm²
|
Baseline and 12 months
|
|
Left ventricular ejection fraction (LVEF)
時間枠:Baseline and 12 months
|
Assessed by CMR, Percentage (%)
|
Baseline and 12 months
|
|
Left ventricular end-diastolic volume (LVEDV)
時間枠:Baseline and 12 months
|
Assessed by CMR, mL
|
Baseline and 12 months
|
|
Left ventricular end-systolic volume (LVESV)
時間枠:Baseline and 12 months
|
Assessed by CMR, mL
|
Baseline and 12 months
|
|
Left ventricular mass (LVM)
時間枠:Baseline and 12 months
|
Assessed by CMR, grams (g)
|
Baseline and 12 months
|
|
LV mass-to-volume ratio (concentricity)
時間枠:Baseline and 12 months
|
Assessed by CMR, g/mL
|
Baseline and 12 months
|
|
Global longitudinal strain (GLS)
時間枠:Baseline and 12 months
|
Assessed by CMR, Percentage (%)
|
Baseline and 12 months
|
|
Superficial retinal capillary plexus vessel density
時間枠:Baseline and 12 months
|
Assessed by OCT-A, Percentage (%)
|
Baseline and 12 months
|
|
Deep retinal capillary plexus vessel density
時間枠:Baseline and 12 months
|
Assessed by OCT-A, Percentage (%)
|
Baseline and 12 months
|
|
Foveal avascular zone (FAZ) area
時間枠:Baseline and 12 months
|
Assessed by OCT-A, mm2
|
Baseline and 12 months
|
|
FAZ perimeter
時間枠:Baseline and 12 months
|
Assessed by OCT-A, mm
|
Baseline and 12 months
|
|
PROMIS Cognitive Function Short Form 8a score
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
|
協力者と研究者
スポンサー
スポンサー
研究記録日
主要日程の研究
研究開始 (推定)
研究開始
一次修了 (推定)
一次修了
研究の完了 (推定)
研究の完了
試験登録日
最初に提出
最初に提出
QC基準を満たした最初の提出物
QC基準を満たした最初の提出物
最初の投稿 (実際)
最初の投稿
学習記録の更新
投稿された最後の更新 (実際)
投稿された最後の更新
QC基準を満たした最後の更新が送信されました
QC基準を満たした最後の更新が送信されました
最終確認日
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
- 薬物の生理学的影響
- 薬理作用の分子機構
- ホルモン
- ホルモン、ホルモン代替品、ホルモン拮抗薬
- 神経伝達物質エージェント
- 膜輸送モジュレーター
- 神経伝達物質取り込み阻害剤
- セロトニン剤
- アミノ酸、ペプチド、およびタンパク質
- 有機化学物質
- 医薬品準備
- 投与形態
- 薬理学的行動
- 化学作用と用途
- 炭化水素
- Cyclohexanes
- シクロパラフィン
- 炭化水素、環状
- 炭化水素、周期的
- 酸、非環式
- カルボン酸
- 多環式化合物
- アミン
- アミノ酸
- ステロイド
- 融合リング化合物
- Estrenes
- エストラン
- エストラジオール同族体
- ゴナダルステロイドホルモン
- ゴナダルホルモン
- ガンマアミノ酪酸
- アミノ酪酸
- 酪酸
- 複雑な混合物
- 酸、炭素環
- コロイド
- シクロヘキサンカルボン酸
- ガバペンチン
- エストラジオール
- 選択的セロトニン再取り込み阻害剤
- フェゾリン
- ゲル
- oxybutynin
その他の研究ID番号
その他の研究ID番号
- MP-37-2026-12489
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
医薬品およびデバイス情報、研究文書
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