The PREDICTOR Study: Assessing Diagnostic Predictors of Airway Collapse in Patients With Obstructive Sleep Apnea

Purpose

This study is an exploratory, multicenter study of up to 300 subjects diagnosed with obstructive sleep apnea who are being evaluated for airway surgery. Subjects will undergo standard evaluation for airway surgery as part of standard of care. In addition to the standard airway assessment, a simple, non-invasive measurement of the width of the inside of each subjects mouth will be performed. This measurement takes 2-3 minutes to perform.

Condition

  • Sleep Apnea, Obstructive

Eligibility

Eligible Ages
Over 18 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Patient meets the indications for the Inspire Upper Airway Stimulation - Patient is being evaluated by drug-induced sleep endoscopy as standard-of-care diagnostic for OSA surgery.

Exclusion Criteria

  • Patient is unable to lie supine for 2-3 minutes in order to undergo airway measurement - Any other reason the investigator deems that the patient is unfit for participation in the study.

Study Design

Phase
N/A
Study Type
Interventional
Allocation
N/A
Intervention Model
Single Group Assignment
Primary Purpose
Diagnostic
Masking
None (Open Label)

Recruiting Locations

Vanderbilt University Medical Center
Nashville, Tennessee 37232
Contact:
Katherine Hartley
katherine.e.hartley@vumc.org

More Details

Status
Recruiting
Sponsor
Inspire Medical Systems, Inc.

Study Contact

Anna N Bader
763-290-1174
annabader@inspiresleep.com

Detailed Description

The objective of the study is to determine whether pharyngeal width (inside of the mouth) is an appropriate measurement to predict absence of complete concentric collapse (CCC) at the soft palate