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临床试验/NCT05981183
NCT05981183招募中不适用

A Single Center Pilot Study on the Use of a Transcutaneous Auricular Vagus Nerve Stimulation Device in CKD Population

NYU Langone Health1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2023年8月9日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
20
试验地点
1
主要终点
Heart Rate Variability (HRV) at Baseline

研究概览

简要总结

The purpose of this pilot interventional study is to collect preliminary data on the application of a transcutaneous auricular vagal nerve stimulation (taVNS) device in patients with chronic kidney disease (CKD). This data will enhance understanding of the short-term safety, tolerability and effects of this novel therapeutic approach in the setting of CKD. The primary aims are to investigate the feasibility of the protocol and generate preliminary signals of efficacy and tolerability for two different doses of vagal nerve stimulation. The pilot estimates will be used to design a larger scale study that may lead to potentially targeted interventions to reduce cardiovascular (CV) mortality in the CKD population.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Individual 18-80 years of age with CKD stage 3-5 (eGFR <60 mL/min/1.73m2) on most recent outpatient labs.

排除标准

  • Pacemaker dependent
  • Prisoners
  • Pregnant women. A pregnancy test will be offered if a subject is concerned about being pregnant.
  • Not capable of informed consent
  • Know autonomic function disorder (e.g. Parkinson's disease with autonomic dysfunction)
  • ICD or PPM precluding assessment of heart rate variability (e.g. chronic atrial fibrillation)
  • Recent myocardial infarction (4 weeks or less)
  • Maintenance dialysis
  • Patients on labetalol (labetalol will interfere with catecholamine measurements)
  • Patients with diabetes
  • At least 50% of cohort must not be on beta blockers. This will help to distinguish the confounding effects of beta blockers.

结局指标

主要结局

Heart Rate Variability (HRV) at Baseline

时间窗: Day 1 (15 minutes prior to administration of intervention)

HRV is the variation in the time interval between heartbeats.

HRV at Post-Intervention

时间窗: Day 1 (15 minutes Post-Intervention)

HRV is the variation in the time interval between heartbeats.

次要结局

  • Blood Pressure at Post-Intervention(Day 1 (15 minutes Post-Intervention))
  • Percentage of Participants with at least a 20% change in HRV from baseline to post-intervention(Day 1 (Up to 15 Minutes Post-Intervention))
  • Heart Rate at Baseline(Day 1 (15 minutes prior to administration of intervention))
  • Blood Pressure at Baseline(Day 1 (15 minutes prior to administration of intervention))
  • Heart Rate at Post-Intervention(Day 1 (15 minutes Post-Intervention))
  • Spontaneous Baroreceptor Sensitivity (BRS) at Baseline(Day 1 (15 minutes prior to administration of intervention))
  • Spontaneous BRS at Post-Intervention(Day 1 (15 minutes Post-Intervention))

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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