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临床试验/NCT02880683
NCT02880683已完成不适用

Cardiac Output Autonomic Stimulation Therapy for Heart Failure (COAST-HF) - Human NeuroCatheter Study

NeuroTronik Inc.1 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2015年10月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
16
试验地点
1
主要终点
Cardiac output

研究概览

简要总结

A single-center feasibility study in patients undergoing cardiac catheterization, to investigate the acute hemodynamic effects of transvenous cardiac autonomic nerve stimulation.

详细描述

A single-center feasibility study performed in patients undergoing a planned cardiac catheterization. This study investigated the feasibility of the NeuroTronik CANS Therapy™ System to improve acute hemodynamics. Purpose-built stimulation catheters were percutaneously inserted into an upper venous structure near the heart via right femoral vein and or left subclavian vein access using standard introducers and techniques. Subjects were instrumented with left ventricular and femoral artery catheters for pressure measurement and stimulated for approximately 60 minutes. Baseline hemodynamic measures were collected before stimulation and compared to measured values during stimulation. Following completion of the protocol, all in-dwelling equipment and catheters were removed.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
盲法
None

入排标准

年龄范围
21 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Stable symptomatic heart failure - New York Heart Association Class II or III
  • Normal Sinus Rhythm

排除标准

  • Unable to gain arterial or venous access using standard percutaneous techniques
  • New York Heart Association Class IV
  • Patient taking amiodarone or other anti-arrhythmic therapy
  • Patients with implanted pacemaker, ICD, or CRT device
  • Patients who had CABG, PCI or enzyme-positive MI within prior month
  • Patients with pre-existing carotid artery or cerebral disease
  • Patients with hypertrophic obstructive cardiomyopathy or infiltrative cardiomyopathy (e.g. amyloidosis, sarcoidosis)
  • Patients who have been hospitalized for heart failure and who required the use of heart failure IV therapy within 30 days before enrollment (measured from release)
  • Patients with current or prior vagal nerve simulator
  • Patients with renal failure
  • Patients with hepatic failure
  • Patients with narrow angle glaucoma
  • Patients who are pregnant
  • Patients with a life expectancy < 12 months per physician judgment
  • Patients with allergy to fentanyl, midazolam, propofol, eggs, egg products, soybeans, or soy products

结局指标

主要结局

Cardiac output

时间窗: One hour

次要结局

  • Arterial blood pressure(One hour)
  • Left ventricular pressure(One hour)
  • Heart rate(One hour)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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