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麦芽糖铁对急性心力衰竭和缺铁患者运动能力和生活质量的影响(COREVIVE-HFrEF) (COREVIVE-HFrEF)

2026年11月4日 更新者:Jingyi Ren、China-Japan Friendship Hospital

出院前给予稳定的急性心力衰竭和缺铁患者服用铁麦芽糖对运动能力和生活质量的影响:一项随机、平行组、双盲、安慰剂对照试验 (COREVIVE-HFrEF)

This study will address whether the additional use of Ferric Derisomaltose on top of standard care will improve exercise capacity and quality of life in patients with acute heart failure and iron deficiency. One group of participants will receive treatment with Ferric Derisomaltose and the other group will receive normal saline 0.9% as placebo.

研究概览

详细说明

Acute heart failure (AHF) is a very common medical problem. Despite improvements in treatment, many patients suffer limiting exercise capacity and quality of life. Previous comorbidities may account for it. Approximately 80% of patients hospitalized with AHF suffered from a combination of iron deficiency. A decline in exercise capacity may occur under this condition. Some research studies have suggested that giving CHF patients intravenous iron improves symptoms in the short term. It is unknown, however, whether correcting iron deficiency is beneficial to patients with AHF to improve excise capacity and whether it improves quality of life and accelerate recovery from acute duration. This study will help us answer these key questions.

This is an investigator-initiated, randomised, parallel group, double-blind, placebo-controlled trial, evaluating the excise capacity improvement of using ferric derisomaltose versus placebo in hospitalized patients with acute heart failure with reduced ejection fraction before discharge.

Participants will be assessed daily using 6-minute walking test after IV iron injection until discharge from hospital, especially focus on the change from baseline to the 3rd day. Some questionnaires are also conducted to evaluate the self-reported status. Participants will be followed up at 2 weeks and 4 weeks.

The primary and secondary endpoints will be examined in subgroups predefined by baseline variables reflecting demography, Hb level, etiology of HF, left ventricular ejection fraction, natriuretic peptide, index of iron metabolism, eGFR and others.

研究类型

介入性

注册 (估计的)

146

阶段

  • 第四阶段

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

  • 姓名:Ying Zhou, Dr
  • 电话号码:+86-13699164283
  • 邮箱:929352903@qq.com

研究联系人备份

  • 姓名:Peizhao Li, Dr
  • 电话号码:+86-18443151740
  • 邮箱:lipz7014@163.com

学习地点

    • Beijing Municipality
      • Beijing、Beijing Municipality、中国
        • 招聘中
        • China-Japan Friendship Hospital
        • 接触:

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  1. Age ≥18 years.

  2. Clinical diagnosis of heart failure with reduced ejection fraction (HFrEF), defined as documented 2-dimensional echocardiography left ventricular ejection fraction (LVEF) <50% before randomization.

  3. Currently hospitalised for an episode of acute heart failure (AHF) where AHF was the primary reason for hospitalisation, New York Heart Association (NYHA) class II - IV.

  4. Reaching hemodynamic stability after standard treatment (if tolerated, initiate four pillars of guideline-directed medical therapies). All of the following (i.e., items a to c) must apply:

    1. Systolic blood pressure≥100mmHg, without symptoms of hypotension;
    2. Stop using intravenous diuretics;
    3. Neither intravenous inotropic drugs or vasodilators were used (including nitrates).
  5. Subject is iron deficient defined as serum ferritin <100 ng/mL or 100 ng/mL ≤ serum ferritin ≤299 ng/mL if TSAT <20%.

  6. Able and willing to provide informed consent and accomplish 6 minutes-walking test.

Exclusion Criteria:

  1. Hematological criteria: ferritin >400 ug/L; hemoglobin <9.0, hemoglobin >13.5 g/dL in women or >14.5 g/dL in men.
  2. Renal dialysis or MDRD/CKD-EPI estimated glomerular filtration rate (eGFR) <15ml/min/1.73m2
  3. Body weight <35kg at randomization.
  4. Heart failure was secondary to valvular diseases or congenital heart diseases.
  5. History of acquired iron overload or hemochromatosis (or first-degree relative of hemochromatosis)
  6. Known hypersensitivity reaction to any component of ferric derisomaltose (Monofer®) or any of its excipients (water for injections, sodium hydroxide (for pH adjustment), hydrochloric acid (for pH adjustment)).
  7. Non-iron deficiency anaemia.
  8. Already receiving erythropoiesis stimulating agents (ESA) or other iron supplements in previous 4 weeks prior to randomization.
  9. Active infection (defined as currently treated with oral or intravenous antibiotics), bleeding (gastrointestinal haemorrhagia, menorrhagia, history of peptic ulcer with no evidence of healing or inflammatory bowel disease) and history of malignant tumor.
  10. Any of the following diseases that hinders exercise testing: severe musculoskeletal disease, unstable angina, obstructive cardiomyopathy, severe uncorrected valvular disease, or uncontrolled slow or rapid arrhythmia (mean ventricular rate> 100 beats / min at rest).
  11. Known positive HBsAg and/or HCV RNA; known HIV positivity; chronic liver disease (including active hepatitis), hepatic sclerosis, ALT or AST > 3x upper limit of normal.
  12. Within 3 months of any of the following: acute myocardial infarction (AMI) or acute coronary syndrome (ACS), transient ischemic attack (TIA) or stroke, uncontrolled hypertension.
  13. Revascularization therapy (coronary artery bypass grafting, percutaneous intervention, or major surgery) in the past 3 months; or planning cardiac surgery or revascularization.
  14. Baseline 6 minutes-walking distance>500m.
  15. Treated with long-term oral high-dose or steroid-immunosuppression therapy.
  16. Investigator considers a possible alternative diagnosis to explain the patient's HF symptoms: severe obesity, primary pulmonary hypertension, or chronic obstructive pulmonary disease (COPD).
  17. Subject is pregnant (e.g., positive human chorionic gonadotropin test) or breast feeding.
  18. Untreated hypothyroidism.
  19. Currently enrolled in any other investigational device or drug study <30 days prior to screening, or received other investigational agent(s).

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:双倍的

武器和干预

参与者组/臂
干预/治疗
实验性的:Ferric derisomaltose

Iron to be administered as ferric derisomaltose.

The treatment dose (mL) to be administered will be determined by the patient's body weight and hemoglobin (Hb) value.

Where Hb ≥10 g/dL, dosage according to body weight is as follows:

Body weight <50 kg: 20 mg/kg; Body weight 50 to <70 kg: 1000 mg; Body weight ≥70 kg: 20 mg/kg up to a maximum of 1500 mg.

Where Hb <10 g/dL, dosage according to body weight is as follows:

Body weight <50 kg: 20 mg/kg; Body weight 50 to <70 kg: 20 mg/kg; Body weight ≥70 kg: 20 mg/kg up to a maximum of 2000 mg.

Infused over a minimum of 15mins for doses up to and including 1000mg, and a minimum of 30 mins for doses >1000mg

After baseline assessments patients will be randomised in a 1:1 ratio to receive ferric derisomaltose IV or placebo (normal saline). In the Treatment group, Ferric derisomaltose will be administered according to the dosing schedule.

其他名称:
  • 单体
  • 铁(III)异麦芽糖苷 1000
安慰剂比较:Placebo

Participants in this arm will receive normal saline 0.9% in analogy to treatment arm.

In the placebo group, patients will receive the equivalent number of normal saline injections.

其他名称:
  • 生理盐水

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Change in 6-minute walking distance
大体时间:Up to 3 days

The difference of 6-minute walking distance in meters from baseline to day3 after IV iron injection.

Up to 3 days

次要结果测量

结果测量
措施说明
大体时间
Change From Baseline in 6-minute walking distance
大体时间:At 2 weeks, 4weeks after IV iron injection

The difference of 6-minute walking distance in meters from baseline at 2 weeks, 4weeks after IV iron injection.

At 2 weeks, 4weeks after IV iron injection
Change From Baseline in the KCCQ Clinical Summary Score
大体时间:At 2 weeks, 4weeks after IV iron injection

KCCQ was a 23-item, self-administered questionnaire that measure the participant's perception of their health status, including their heart failure (HF) symptoms, impact on physical and social function and how their HF impacts the quality of life. KCCQ quantifies 7 domains: physical limitations (6 items), symptom stability (1 item), symptom frequency (4 items), symptom burden (3 items), self-efficacy (2 items), quality of life (3 items) and social limitations (4 items). Scores were generated for each domain and scaled from 0 to 100, with 0 denoting the worst and 100 the best possible status. KCCQ-clinical summary score was average of domains- physical limitation and total symptoms (average of symptom frequency and symptom burden), and transformed to a single score which ranged from 0 (worst) -100 (the best possible status), where the higher score reflected better health status.

At 2 weeks, 4weeks after IV iron injection
Change From Baseline in the EQ-5D-5L Questionnaire Indexed Value
大体时间:At 3 days, 2weeks, 4weeks after IV iron injection

EQ-5D-5L: European Quality of Life-5 Dimensions-5 Levels The EQ 5D questionnaire consists of a health descriptive system for participants to self-classify and rate their health status on the day of administration.

The descriptive system includes 5 items/dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression, which are coded from 1 (best state) to 5 (worst state).

At 3 days, 2weeks, 4weeks after IV iron injection
Change From Baseline in NYHA Functional Class
大体时间:At 3 days, 2weeks, 4weeks after IV iron injection

NYHA = New York Heart Association

NYHA functional class was assessed as Class I, II, III, IV:

Class I - No symptoms and no limitation in ordinary physical activity, e.g. shortness of breath when walking, climbing stairs etc.

Class II - Mild symptoms (mild shortness of breath and/or angina) and slight limitation during ordinary activity.

Class III - Marked limitation in activity due to symptoms, even during less-than-ordinary activity. Comfortable only at rest.

Class IV - Severe limitations. Experiences symptoms even while at rest.

Lower response categories are better for score NYHA.

At 3 days, 2weeks, 4weeks after IV iron injection
Change From Baseline in PGA quality of life questionnaire
大体时间:At 3 days, 2weeks, 4weeks after IV iron injection

PGA:Patient Global Assessment

PGA questionnaire consists of a health descriptive system for participants to self-reported and rate their medical condition after participate this study.

The descriptive system includes 7 choices:has much improved, has (moderately) improved, has a little improved, is unchanged, is a little worse, is (moderately) worse, is much worse, which are coded from 1 (best state) to 7 (worst state).

At 3 days, 2weeks, 4weeks after IV iron injection
Change From Baseline in Concentration of hemoglobin (Hb)
大体时间:At 3 days, 2weeks, 4weeks after IV iron injection

Hemoglobin (Hb) is a commonly used clinical test for assessing anaemia, with units of g/L.

At 3 days, 2weeks, 4weeks after IV iron injection
Change From Baseline in proportion of reticulocyte (Ret%)
大体时间:At 3 days, 2weeks, 4weeks after IV iron injection

The reticulocyte ratio is often used to reflect the hematopoiesis of the bone marrow erythrocyte with units of percentage(%).

At 3 days, 2weeks, 4weeks after IV iron injection
Change From Baseline in Concentration of ferritin
大体时间:At 3 days, 2weeks, 4weeks after IV iron injection

To assess the effect of ferric derisomaltose vs. placebo on change in ferritin from baseline to 3 days, 2weeks and 4weeks

At 3 days, 2weeks, 4weeks after IV iron injection
Change From Baseline in concentration of transferrin saturation
大体时间:At 3 days, 2weeks, 4weeks after IV iron injection

To assess the effect of ferric derisomaltose vs. placebo on change in transferrin saturation from baseline to 3 days, 2weeks and 4weeks

At 3 days, 2weeks, 4weeks after IV iron injection
Change From Baseline in Concentration of serum transferrin receptors (sTfR)
大体时间:At 3 days, 2weeks, 4weeks after IV iron injection

To assess the effect of ferric derisomaltose vs. placebo on change in serum transferrin receptors (sTfR) from baseline to 3 days, 2weeks and 4weeks

At 3 days, 2weeks, 4weeks after IV iron injection
Change From Baseline in Concentration of N-terminal Pro-brain Natriuretic Peptide (NT-proBNP)
大体时间:At 3 days, 2weeks, 4weeks after IV iron injection

To assess the effect of ferric derisomaltose vs. placebo on change in NT-proBNP from baseline to 3 days, 2weeks and 4weeks

At 3 days, 2weeks, 4weeks after IV iron injection
Change From Baseline in Left Ventricular Systolic Function
大体时间:At 2weeks, 4weeks after IV iron injection

Left ventricular ejection fraction is assessed by two-dimensional directed M-mode echocardiography.

At 2weeks, 4weeks after IV iron injection
Change From Baseline in Left Ventricular End-Diastolic Diameter
大体时间:At 2weeks, 4weeks after IV iron injection

Left ventricular end-diastolic diameter is assessed by two-dimensional directed M-mode echocardiography.

At 2weeks, 4weeks after IV iron injection

其他结果措施

结果测量
措施说明
大体时间
Change From Baseline in Urine Albumin-to-Creatinine Ratio (UACR)
大体时间:At 3 days, 2weeks, 4weeks after IV iron injection

Urine Albumin-to-Creatinine Ratio (UACR) is regard as a safety endpoint to reflect early injury of kidney.

At 3 days, 2weeks, 4weeks after IV iron injection
A rise of high-sensitivity C-reaction protein (hs-CRP) levels from baseline
大体时间:Up to 4weeks

Safety endpoint is defined as a rise of high-sensitivity C-reaction protein (hs-CRP) from baseline.

Up to 4weeks
Adverse Event after IV iron injection
大体时间:Up to 4weeks

Adverse Event Include Fishbane symptoms (flushing/chest pain/back pain/chest tightness, sometimes with dyspnea), isolated signs and symptoms (urticaria/pruritus/rash/mild hypotension, hypertension/tachycardia/nausea/headache), signs and symptoms of allergic reactions (persistent hypotension; airway angioedema/generalised urticaria, non-airway angioedema/wheezing, bronchospasm, vomiting, abdominal pain, etc.)

Up to 4weeks

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2023年8月1日

初级完成 (估计的)

2027年8月1日

研究完成 (估计的)

2027年8月1日

研究注册日期

首次提交

2023年7月13日

首先提交符合 QC 标准的

2023年7月25日

首次发布 (实际的)

2023年8月2日

研究记录更新

最后更新发布 (实际的)

2026年11月6日

上次提交的符合 QC 标准的更新

2026年11月4日

最后验证

2026年11月1日

更多信息

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研究美国 FDA 监管的设备产品

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在美国制造并从美国出口的产品

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