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临床试验/NCT06283017
NCT06283017已完成不适用

Acute Proof-of-Concept Study to Evaluate Hypoglossal Nerve Stimulation in Humans With Obstructive Sleep Apnea

Invicta Medical Inc.2 个研究点 分布在 1 个国家目标入组 14 人开始时间: 2022年4月6日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
14
试验地点
2
主要终点
Safety outcomes

研究概览

简要总结

This proof-of-concept study is being performed to evaluate whether the hypoglossal nerve can be stimulated using a small series of electrodes placed surgically via a percutaneous approach. Minimally invasive off the shelf medical devices will be used and observation of the characteristic physiological responses to stimulation of the HGN, will be assessed.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Basic Science
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

  • Subject must be eligible for a diagnostic or surgical procedure and
  • Suffers from OSA (apnea/hypopnea index >10 event/h sleep) based on history and a physical exam.
  • Is a surgical candidate.
  • Is willing and capable of providing informed consent.
  • Is willing to have a representative electrode array temporarily placed in the submandibular and mylohyoid space.
  • Is willing to participate in the designated follow-up visits.
  • Must be in good general health.
  • Is able to understand and has voluntarily signed and dated the IRB or EC approved informed consent form (ICF) prior to initiation of any screening or study-specific procedure.
  • Must be minimum of 18 years and maximum 80 years of age.

排除标准

  • Has Body Mass Index above 35 kg/m
  • Has had surgical resection or radiation therapy for cancer or congenital malformations in the larynx, tongue, or throat.
  • Has significant co-morbidities making them unable or inappropriate to participate in this POC study.

研究组 & 干预措施

Hypoglossal nerve stimulation

Experimental

Device-mediated stimulation of the hypoglossal nerve

干预措施: Hypoglossal nerve stimulation (Device)

结局指标

主要结局

Safety outcomes

时间窗: Day 30

To evaluate and report all observed adverse events, serious adverse events, unanticipated adverse events and adverse device effects observed during the study

Characterization of lead placement outcomes

时间窗: Day 0

Spatial characterization of the orientation of the electrode array and lead body to the target stimulation location considering suitable chronic anchoring locations.

Lead placement and removal outcomes

时间窗: Day 0

To demonstrate the ability to safely place and remove the electrode array, per protocol instructions.

Target identification and access outcomes

时间窗: Day 0

Identification of and access to the target stimulation location aligned with the medial branch of the Hypoglossal Nerve

Tongue protrusion outcomes

时间窗: Day 0

Visual verification of protrusion of the tongue during stimulation at the target stimulation location with a representative electrode array.

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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