Snoring Clinical Trial - The Effect of the DryMouth Shield on Snoring

Status Terminated

Clinical Trial Summary

To measure the effect of the DryMouth Shield on snoring.

Clinical Trial Description

The primary outcome of this study is to aid in the final design of the DryMouth Shield and to assess the effect of the DryMouth Shield on snoring frequency. To accomplish this we will compare the frequency of snores during 1) overnight polysomnography without using the DryMouth Shield and 2) overnight polysomnography using the DryMouth Shield. Secondary outcomes of the study will include: 1) compare the difference in the volume of snores without and with the use of the DryMouth Shield; 2) estimate the changes in apnea hypopnea index without and with the use of the DryMouth Shield; 3) describe symptoms of dry mouth without and with the use of the DryMouth Shield 4) describe symptoms of bruxism without and with the use of the dry mouth shield and 5) gather patient feedback about the user experience with the dry mouth shield. ;

Study Design

Related Conditions & MeSH terms

Snoring

Clinical Trial Details

NCT number	NCT03701165
Study type	Interventional
Source	VMS Medical Products, Inc
Contact
Status	Terminated
Phase	N/A
Start date	October 15, 2018
Completion date	January 31, 2019

View Details

See also
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