跳至主要内容
临床试验/NCT01720160
NCT01720160Unknown不适用

Barostim HOPE4HF Study

CVRx, Inc.46 个研究点 分布在 1 个国家目标入组 98 人开始时间: 2012年11月最近更新:
适应症
干预措施

试验速览

阶段
不适用
发起方
CVRx, Inc.
入组人数
98
试验地点
46
主要终点
Heart failure metric improvements from baseline

研究概览

简要总结

The purpose of this clinical investigation is to assess the long-term safety and efficacy of the BAROSTIM NEO System in subjects currently participating in the BAROSTIM® HOPE4HF Trial (NCT01720160).

详细描述

A prospective, randomized study describing the safety and efficacy of the BAROSTIM NEO System in heart failure subjects with left ventricular ejection fraction equal to or less than 35 percent. Seventy two subjects were randomized; 32 to the medical management arm and 40 to the device arm (38 implanted, 2 withdrawn). The study closed to new enrollments on January 31, 2014. Subjects are in long-term follow-up and are required to have at least one annual visit. During the visit, there will be a physical assessment, a review of medications and serious adverse events.

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
None

入排标准

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

入选标准

  • Actively participating in the BAROSTIM HOPE4HF Study and currently implanted with the BAROSTIM NEO device with the device turned ON.
  • Have signed a revised approved informed consent form for continued participation in this study.

排除标准

  • Treating physician decision that the subject should not continue with therapy.

研究组 & 干预措施

Device

Experimental
  1. BAROSTIM NEO System and 2) standard of care medical management therapy for heart failure (American Heart Association [AHA] / American College of Cardiology [ACC] guidelines), including drugs (determined by the patient's physician). Drug types include: Loop Diuretics, Thiazide Diuretics, Potassium-sparing Diuretics, Sequential Nephron Blockade, ACE Inhibitors, ARBs, ARNI, Aldosterone Antagonists, Beta Blockers and Hydralazine and Isosorbide Dinitrate.

干预措施: BAROSTIM NEO® System (Device)

Device

Experimental
  1. BAROSTIM NEO System and 2) standard of care medical management therapy for heart failure (American Heart Association [AHA] / American College of Cardiology [ACC] guidelines), including drugs (determined by the patient's physician). Drug types include: Loop Diuretics, Thiazide Diuretics, Potassium-sparing Diuretics, Sequential Nephron Blockade, ACE Inhibitors, ARBs, ARNI, Aldosterone Antagonists, Beta Blockers and Hydralazine and Isosorbide Dinitrate.

干预措施: Standard of care medical managment therapy for heart failure (Other)

Medical Management

Active Comparator

Standard of care medical management therapy for heart failure (American Heart Association [AHA] / American College of Cardiology [ACC] guidelines), including drugs (determined by the patient's physician). Drug types include: Loop Diuretics, Thiazide Diuretics, Potassium-sparing Diuretics, Sequential Nephron Blockade, ACE Inhibitors, ARBs, ARNI, Aldosterone Antagonists, Beta Blockers and Hydralazine and Isosorbide Dinitrate.

干预措施: Standard of care medical managment therapy for heart failure (Other)

结局指标

主要结局

Heart failure metric improvements from baseline

时间窗: 12 months

To describe changes in measures compared to baseline.

System and procedure related adverse events

时间窗: 6 months

To demonstrate the safety of the Neo system in a heart failure population.

次要结局

未报告次要终点

研究者

发起方
CVRx, Inc.
申办方类型
Industry
责任方
Sponsor

研究点 (46)

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