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临床试验/NCT03589846
NCT03589846Enrolling By Invitation不适用

The Effect of Palatoglossus and Genioglossus Stimulation During Drug-Induced Sleep Endoscopy

Vanderbilt University Medical Center2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2018年7月26日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
Enrolling By Invitation
入组人数
60
试验地点
2
主要终点
Basic physiologic measurements

研究概览

简要总结

Drug-induced sleep endoscopy (DISE) is a widely used tool for assessing collapse patterns of the upper airway anatomy during sleep. Hypoglossal nerve stimulation therapy for obstructive sleep apnea suffers from variable response at the level of the soft palate. We propose a study examining the physiologic effect of palatoglossus and genioglossus muscle stimulation during DISE.

详细描述

This is a single-arm study involving the use of a diagnostic device (muscle stimulator) that is not currently utilized in any clinical decision-making processes for OSA patients. All patients scheduled for DISE as part of their regular clinical care will be screened for enrollment via the previously described inclusion and exclusion criteria. The study is not blinded. No diagnostic information collected from muscle stimulation will be used in clinical decision-making processes.

研究设计

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

  • Adult patient (≥18 years old)
  • A diagnosis of obstructive sleep apnea as determined by polysomnogram with an apnea-hypopnea index of ≥ 5.0/hr.
  • Intolerant of CPAP therapy due to physical or psychosocial limitations as determined by clinical history
  • Scheduled to undergo DISE as part of routine clinical assessment for further evaluation of pharyngeal anatomy

排除标准

  • Unable to consent for research due to a pre-existing neurologic condition as determined by PI
  • Unable to consent for research due to language barriers
  • A history of egg allergy as determined by history or self-reports
  • Currently pregnant as determined by patient report or pre-operative anesthesia evaluation
  • Cardiopulmonary or other medical conditions precluding safe propofol sedation as determined by pre-operative anesthesia evaluation
  • History of palatal or pharyngeal airway surgery including tonsillectomy as determined by clinical history and exam
  • History of radiation treatment to the head or neck as determined by history and/or physical exam

研究组 & 干预措施

Muscle stimulation

Experimental

Consented participants who meet eligibility will have a drug induced sleep endoscopy (DISE) and the Grass S88 muscle stimulator.

干预措施: Grass S88 Muscle Stimulator (Device)

结局指标

主要结局

Basic physiologic measurements

时间窗: Collected during operative procedure, taking about 15 minutes.

This study involves the collection of basic physiologic measurements (airway cross-sectional diameter with and without muscle stimulation) during a single session of DISE.

次要结局

  • Amount of current needed for adequate stimulation(Collected during operative procedure, taking about 15 minutes.)

研究者

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

David Kent

Assistant Professor, Department of Otolaryngology

Vanderbilt University Medical Center

研究点 (2)

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