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临床试验/NCT07417215
NCT07417215已完成4 期

The Effect of Sacubitril and Valsartan on Heart Function in Chronic Hemodialysis Patients With HFpEF

University Clinical Hospital Mostar1 个研究点 分布在 1 个国家目标入组 52 人开始时间: 2026年1月30日最近更新:
干预措施

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
52
试验地点
1
主要终点
Change in left atrial volume index (LAVI)

研究概览

简要总结

Heart failure is the most common cause of death of patients on chronic hemodialysis treatment, and to date there is no effective therapy for the treatment of this comorbidity in this group of patients. The most common form of heart failure in these groups of patients is heart failure with preserved ejection fraction (HFpEF). As a new therapy for heart failure, a new group of drugs called angiotensin receptor and neprilysin inhibitors (ARNI) has been imposed, whose representative is the drug sacubitril/valsartan. The therapy has been shown to be superior to any other therapy to date for the treatment of heart failure with reduced ejection fraction (HFrEF) and has been included in European and American guidelines for the treatment of patients with HFrEF. Since 2022, the drug has been approved in the USA for the treatment of patients with HFpEF, while in Europe it is still not approved for this indication.

Currently, the drug is not approved for patients on chronic hemodialysis anywhere in the world, and its effect on this group of patients is unknown. There are very few studies examining the safety and efficacy of sacubitril/valsartan in chronic hemodialysis patients with HFpEF. Precisely because of this, the aim of this study is to determine the effectiveness of this drug in these groups of patients. I will conduct the research as a randomized controlled trial (single blind research) where the subjects will be patients on chronic hemodialysis treatment who have proven HFpEF. HFpEF is proven by the HFA-PEFF scale. The patients will be divided into two groups - the test group and the control group (30 patients in each group). The input variables will be patients on chronic hemodialysis treatment (whose hemodialysis treatment lasts at least one year); patients with heart failure with preserved ejection fraction; height; weight. Output variables will be heart ultrasound parameters and laboratory findings (NTproBNP, hs troponin, aldosterone, renin). The aim of the study is to determine the effect of sacubitril/valsartan on ultrasound parameters and on cardiovascular and other biomarkers in patients on chronic hemodialysis treatment with HFpEF.

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
Single (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

  • patients on chronic hemodialysis treatment (minimum 1 year); confirmed diagnosis of HFpEF; systolic arterial pressure >100 mmHg.

排除标准

  • patients not on chronic hemodialysis treatment; patients with unconfirmed diagnosis of HFpEF; patients with systolic blood pressure <100 mmHg; patients unwilling to participate in the study;

研究组 & 干预措施

Standard Therapy for hemodialysis patients

No Intervention

30 patients on chronic hemodialysis who have proven heart failure with preserved ejection fraction will not receive any other medication (they will receive the gold standard)

Experimental - Sacubitril/valsartan

Experimental

30 patients on chronic hemodialysis with proven heart failure with preserved ejection fraction will receive sacubitril/valsartan

干预措施: Sacubitril / Valsartan (Drug)

结局指标

主要结局

Change in left atrial volume index (LAVI)

时间窗: 2 months

Change in left atrial volume index (LAVI), measured by transthoracic echocardiography using the biplane area-length method and indexed to body surface area (mL/m²). LAVI will be calculated according to current echocardiographic guidelines. The outcome is defined as the absolute change in LAVI from baseline to 2 months following initiation of sacubitril/valsartan therapy in the experimental group and during standard therapy in the control group.

次要结局

  • Change in left ventricular global longitudinal strain (LV GLS)(2 months)
  • Change in E/e' ratio(2 months)
  • Change in N-terminal pro-B-type natriuretic peptide (NT-proBNP)(2 months)

研究者

发起方
University Clinical Hospital Mostar
申办方类型
Other
责任方
Principal Investigator
主要研究者

Ivan Zeljko

M. D. ; Principal Investigator

University Clinical Hospital Mostar

研究点 (1)

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