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临床试验/NCT03391141
NCT03391141已完成不适用

In Vivo Aerodynamic Modeling of the Upper Airway in OSA

Dr. Erica Thaler1 个研究点 分布在 1 个国家目标入组 34 人开始时间: 2018年4月9日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
34
试验地点
1
主要终点
site of airway obstruction

研究概览

简要总结

This study aims to validate whether the pattern of airway collapse recorded during Drug-Induced Sleep Endoscopy (DISE) mirrors that of natural sleep, and to develop a model for airway collapse. Sensors will be placed in subjects' upper airways during DISE and then during in-lab sleep studies. The sleep study results will be compared with OR findings to create an aerodynamic model for natural sleep and to assess whether airway observations during DISE were valid representations of natural sleep.

详细描述

Drug-induced sleep endoscopy (DISE) was developed in 1991 as a technique to characterize upper airway collapse in patients with OSA. With the advent of various upper airway surgeries introduced in recent years, DISE has become increasingly utilized by the sleep surgeon as a surrogate for airway collapse during natural sleep in order to tailor a surgical approach for each patient. Propofol and/or midazolam infusions are typically used for sedation in these cases, however, there is limited evidence to suggest that these anesthetics reproduce natural sleep architecture. Therefore, it cannot be assumed that the pattern of collapse observed during DISE is reflective of natural sleep.

The aim of this study is to validate whether the pattern of collapse recorded during DISE mirrors that of natural sleep. Furthermore, the investigators aim to develop a quantitative in vivo model for airway collapse in order to further our understanding of the pathophysiology of OSA. They will do this by comparing the findings from DISE with aerodynamic readings from within the upper airway during natural sleep. The proposed technique will employ technologies already approved by the FDA for clinical use. Capacitance circuitry, airflow sensors, and/or pressure transducers will be suspended within the upper aerodigestive tract along a thin, low-profile, and flexible tube. During Phase I of the study, this aerodynamic probe will be placed in the OR during DISE along the upper airway, namely in the retropalatal, retroglossal, and hypopharyngeal regions. Readings will be correlated and calibrated with DISE findings in real-time. During Phase II, these sensors will again be placed within the same patients during in-office sleep studies. The results from the sleep study will be analyzed in conjunction with OR findings in order to create an aerodynamic model for natural sleep. This will also allow the investigators to assess whether airway observations during DISE were valid representations of natural sleep.

研究设计

研究类型
Observational
观察模型
Cohort
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 with moderate to severe OSAS
  • Must have symptoms of OSAS
  • Must have sleep study showing AHI of 15 or greater
  • Failed trial of CPAP
  • BMI less than 35
  • Be a surgical candidate for ablative or neuro-stimulation surgery
  • Acceptable surgical comorbidities
  • Non-aberrant upper airway anatomy
  • Must demonstrate reliability in keep appointments

排除标准

  • Prior ablative airway surgeries
  • Allergies to oxymetazoline or lidocaine
  • Significant central sleep apnea
  • Presence of other sleep disorders
  • History of neurologic or neuromuscular disease
  • Historical or present substance abuse
  • Bleeding disorders
  • Autoimmune diseases that increase risk of nasal trauma such as Wegener's, Sarcoidosis, etc.
  • Pregnancy
  • Unacceptable anesthesia risk
  • Ablative or orthognathic airway surgery
  • Significant weight loss or weight gain with or without bariatric surgery
  • Initiation of new drug that is known to alter sleep architecture
  • Development of head and neck neoplasm
  • Development of autoimmune disease altering airway anatomy
  • Trauma to head and neck region

结局指标

主要结局

site of airway obstruction

时间窗: 3 months

the presence or absence of airway obstruction in the retropalatal, retroglossal, and hypopharyngeal areas

次要结局

未报告次要终点

研究者

发起方
Dr. Erica Thaler
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Dr. Erica Thaler

Professor

University of Pennsylvania

研究点 (1)

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