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临床试验/NCT03844516
NCT03844516Unknown不适用

Work Intolerance in Left Ventricular Assist Device Recipients: Impact of Pacing

Finn Gustafsson2 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2019年4月23日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
15
试验地点
2
主要终点
Peak oxygen uptake (pVO2)

研究概览

简要总结

Implantation with left ventricular assist device (LVAD) in patients with end-stage heart failure (HF) leads to improvements in survival and quality of life, however, work capacity remains disappointingly low, at half of the expected value. Complex central and peripheral hallmarks of heart failure attribute to the continued work intolerance, to which heart rate may be a contributing factor.

The purpose of this study is to clarify the impact of heart rate (by means of pacing) on work capacity (measured as peak oxygen uptake) in LVAD recipients.

详细描述

While implantation with left ventricular assist devices (LVADs) in patients with end-stage heart failure (HF) improve survival and quality of life, work capacity remains at a disappointing 50% of the expected value.

Due to the worldwide (increasing) shortage of donor hearts, LVADs are increasingly used as destination therapy which makes it crucial for physicians to persistently identify opportunities to improve management, lower the adverse events and maximize the benefits of this treatment option.

In recent years it was found that upregulation of device pump speed improves the maximal work capacity of LVAD recipients with no side effects. More recently it was found that the patients' heart rate reserve also was of importance in this regard, however, the latter was shown in a retrospective study and needs to be confirmed in a prospective randomized double-blinded intervention study. As a large portion of LVAD recipients are already implanted with a pacing device (and suffer from chronotropic incompetence) such a study is possible to conduct by controlling their heart rate during exercise by pacing (ie randomized crossover design).

研究设计

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

盲法说明

Patients and staff performing the peak oxygen uptake test (pVO2) will be blinded to device regulation. Blinding will be ensured by recruiting a secondary doctor or other staff to regulate pace-settings in relation to the paced pVO2 test while performing sham regulations (or just read pace-settings) in relation to the non-paced pVO2 test.

Thus, both patients and investigator are blinded.

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

  • Implanted with a left ventricular assist device
  • Implanted with a pace-device ensuring the possibility of pacing
  • Age > 18

排除标准

  • Not able to undergo a peak oxygen uptake test
  • No consent

结局指标

主要结局

Peak oxygen uptake (pVO2)

时间窗: 1 Day

次要结局

  • Heart rate(1 Day)

研究者

发起方
Finn Gustafsson
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Finn Gustafsson

Professor

Rigshospitalet, Denmark

研究点 (2)

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