跳至主要内容
临床试验/NCT06635265
NCT06635265已完成不适用

Single Center Proof-of-Concept Study to Determine the Flow Changes And/or AHI Reduction When Stimulating Two Targets (neural And/or Muscular) for the Treatment of Obstructive Sleep Apnea in Adult Subjects

Invicta Medical Inc.2 个研究点 分布在 1 个国家目标入组 3 人开始时间: 2023年4月3日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
3
试验地点
2
主要终点
Impacts on acute airway opening

研究概览

简要总结

This Proof-of-Concept study will collect acute and sub-acute flow and/or AHI data following the placement of lead arrays under direct vision. The acute placement and data collection will be collected following the completion of the pre-scheduled neck dissection surgery. The sub-acute data will be collected in a sleep lab during a polysomnography (PSG). Both data collections will be done when stimulating (using an external pulse generator) the hypoglossal nerve or Genioglossus muscle (GG) and a second neural target (Ansa Cervicalis - AC) or the strap muscles (sternohyoid and sternothyroid) with a set of Off-the-Shelf (OTS) electrode arrays.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • A patient must meet all of the following inclusion criteria to be eligible for inclusion in this study:
  • Age above 18 years not under guardianship, under curatorship or under judicial protection.
  • Body Mass Index (BMI) < 38 kg/m
  • Subject must be eligible for neck dissection surgery.
  • Written informed consent obtained from the patient prior to performing any study specific procedure.
  • Willing and capable to comply with all study requirements, including specific lifestyle considerations, evaluation procedures and questionnaires for the whole duration of the trial.

排除标准

  • Patients meeting any of the following criteria will be excluded from participation in this study:
  • Major anatomical or functional abnormalities that would impair the ability of the electrode arrays to be positioned.
  • Significant comorbidities that contraindicate surgery or general anesthesia.
  • Significant tongue weakness.
  • Aerodigestive tract tumor or reconstructive surgery performed at the same time as neck dissection.
  • Any other chronic medical illness or condition that contraindicates a surgical procedure or general anesthesia in the judgment of the investigator.
  • Prior surgery or treatments that could compromise the placement and effectiveness of the electrode array systems:
  • Airway cancer surgery or radiation, or
  • Mandible or maxilla surgery in the previous 3 years (not counting dental treatments).
  • Other upper airway surgery to remove obstructions related to OSA in the previous 3 months (e.g., uvulopalatopharyngoplasty (UPPP), tonsillectomy, nasal airway surgery).
  • Prior hypoglossal nerve stimulation device implantation.
  • Currently pregnant or breastfeeding during the study period.
  • Concomitant oral or pharyngeal surgery.

结局指标

主要结局

Impacts on acute airway opening

时间窗: Day 0 to 3

Demonstration of acute airway opening as visually observed under nasoendoscopy when stimulating the HGN or GG and a second target (neural or direct muscle stimulation).

Impacts on airflow during a acute assessment

时间窗: Day 0 to 3

Acute increase in airflow when stimulating the HGN or GG and a second target (neural or direct muscle stimulation), measured by changes in amplitude (mA) during target stimulation.

次要结局

  • Impacts on airway opening during a sub-acute assessment(Day 0 to 3)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验