跳至主要内容
临床试验/NCT00850980
NCT00850980撤回不适用

Selective AV Nodal Vagal Stimulation For Reduction of the Ventricular Rate During Atrial Fibrillation

The Cleveland Clinic1 个研究点 分布在 1 个国家开始时间: 2009年2月最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
试验地点
1
主要终点
The primary endpoint will be the change in ventricular rate from baseline measured at each amplitude

研究概览

简要总结

The study will enroll patients that are already in AF and in which open-heart surgical intervention has been scheduled. In these patients AVN-VNS will be delivered briefly (minutes) after the incision as a proof-of-concept therapy, with concomitant monitoring of the effects on the ventricular rate.

详细描述

Rate control during AF can be achieved by drugs (Ca++ blockers, digoxin, beta-blockers), or by AV nodal ablation. Drugs, as usual, have limitations, while the radical destruction of the AV node renders the patient permanently pacemaker-dependent.

In series of animal studies the investigators employed AVN-VNS delivered to the so-called AV nodal fat pad. Electrical stimulation of the fat pad resulted in release of neuromediator (acetylcholine) within the AV nodal domain. The investigators have demonstrated that this approach successfully and substantially slowed the ventricular rate during AF in both acute and chronic experiments without inflicting any damage on the AV node.

It is our hypothesis that temporary delivery of selective AVN-VNS in patients with AF will provide the benefits of reduced ventricular rate during the ongoing AF. The proposed study will be limited only to patients that are already in AF and in which open-heart surgical intervention has been scheduled. In these patients AVN-VNS will be delivered briefly (minutes) after the incision as a proof-of-concept therapy, with concomitant monitoring of the effects on the ventricular rate.

Based on the information obtained in this study, the investigators intend subsequently to test the AVN-VNS in a group of patients that develop AF post-operatively and remain in this status for several days after the surgery. A protocol for a separate study will be submitted if and when this becomes feasible.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

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 undergoing open heart surgery
  • Able to give Informed Consent and
  • Permanent/Persistent or currently in Atrial Fibrillation

排除标准

  • Minimally invasive incisions
  • Previous open heart surgery
  • Bleeding diathesis
  • Creatinine levels greater than 2.0 mg/dl
  • Active Infections, i.e. endocarditis
  • Implanted ICD
  • Pregnancy and nursing
  • Incompetence and/or other conditions, which do not allow the patient to understand the nature, significance and scope of the study
  • Patients on drugs that have cholinesterase inhibitor activity (e.g., physostigmine-like substances).

结局指标

主要结局

The primary endpoint will be the change in ventricular rate from baseline measured at each amplitude

时间窗: surgery

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Marc Gillinov, MD

Principal Investigator

The Cleveland Clinic

研究点 (1)

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