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临床试验/NCT05793996
NCT05793996招募中4 期

Study of the Prevalence of Iron Deficiency Among Hospitalized Patients With HFpEF and the Impact of Ferinject® on Indicators of Quality of Life, Functional Status in Patients With Iron Deficiency

Tomsk National Research Medical Center of the Russian Academy of Sciences2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2023年4月28日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
招募中
入组人数
100
试验地点
2
主要终点
Primary Outcome (Combined)

研究概览

简要总结

Observational cohort randomized controlled study to study the influence of correction of ID by intravenous injection of ferric carboxymaltose (Ferinject®) on quality of life indicators, functional status in a cohort of patients with HFpEF.

详细描述

The prevalence of HFpEF among patients admitted to cardiology hospitals will be studied. The study will include patients with NYHA II-III who have signed an informed consent that meets the inclusion/exclusion criteria. The effectiveness of intravenous administration of iron carboxymaltose (Ferinject ® ) to correct iron deficiency and improve the clinical course of HFpEF will be evaluated. A group without iron deficiency will be recruited as a control group (n=30).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Signed informed consent to participate in the study;
  • In New York Heart Association (NYHA) II-III functional class due to stable symptomatic chronic heart failure (CHF);
  • Left ventricular ejection fraction (LVEF) ≥50%; objective signs of structural and/or functional disorders of the heart consistent with the presence of LV diastolic dysfunction/increased LV filling pressure, including elevated levels of natriuretic peptide;
  • Screening ferritin below 100 µg/L, or below 300 µg/L when transferrin saturation (TSAT) is below 20%;
  • Screening haemoglobin (Hb) at the time of switching on ( 90-150 g/l).

排除标准

  • Uncontrolled arterial hypertension;
  • Аnemia not related to iron deficiency;
  • Аnemia with a hemoglobin level of less than 90 g/l;
  • Less than 1 year after acute myocardial infarction;
  • Less than 1 year after acute cerebral circulation disorder;
  • Less than 1 year after surgical interventions, including non-cardiac operations and myocardial revascularization (coronary bypass surgery, coronary artery stenting), operations for valvular pathology;
  • Chronic alcoholism (including alcoholic heart disease), mental disorders;
  • Severe hepatic (increased transaminase levels above the upper three limits of normal) and renal insufficiency (glomerular filtration rate less than 15 ml/min/1.73 m2);
  • Known active infection, clinically significant bleeding, active malignancy;
  • Severe autoimmune diseases (systemic lupus erythematosus, rheumatoid arthritis, etc.);
  • Severe bronchial asthma, COPD in the acute stage;
  • Allergic reactions to medications in the anamnesis, eczema, atopic allergic reaction;
  • Blood transfusions and taking erythropoiesis-stimulating drugs during the previous three months.

研究组 & 干预措施

Experimental: 1

Active Comparator

Drug: Ferinject ® (Ferric carboxymaltose)

干预措施: Ferinject (Drug)

Comparison Group: 2

Other

Diet therapy, without drug therapy

干预措施: Diet therapy (Other)

结局指标

主要结局

Primary Outcome (Combined)

时间窗: 12 months

Change of 5 or more points on the Kansas City Cardiomyopathy Questionnaire (KCCQ) (0-100 points)+change in test distance with a 6-minute walk (6MWD - 150 meters or more) by 35 meters or more. An increase in the number of points by 5 on the Kansas City Cardiomyopathy Questionnaire scale, increasing the distance on the 6-minute walk test by 35 meters means a better result. The absence of changes/decrease in the number of points on the Kansas City Cardiomyopathy Questionnaire scale, the absence of changes/decrease in the distance in the 6-minute walking test means the worst result.

次要结局

  • Hospitalization for heart failure and death from all causes(12 months)
  • Changing by 5 or more points according to the Minnesota Heart Failure Quality of Life Questionnaire (MHFLQ) (0-105 points).(6 months)
  • Changing in test distance with a 6-minute walk (6MWD 300 meters or more) of 35 meters(6 months)
  • Changing functional class of chronic heart failure (CHF) by New York Heart Association (NYHA I-IV functional classes)(6 months)
  • Changing by 5 or more points on the Kansas City Cardiomyopathy Questionnaire (KCCQ 0-100 points)(6 months)

研究者

研究点 (2)

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