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
Status	Clinical Trial	Phase
Recruiting	`NCT05371509` - Novel Myofunctional Water Bottle to Reduce OSA and Snoring Study	N/A
Active, not recruiting	`NCT02470182` - Screening for Sleep Disordered Breathing With Minimally Obtrusive Sensors
Completed	`NCT03964324` - NO Measurements in Screening for Asthma and OSA, in Patients With Severe Snoring	N/A
Completed	`NCT06186687` - Rehabilitative Approaches: Myofunctional Therapy and Retropalatal Narrowing and Snoring	N/A
Completed	`NCT03640793` - Prospective Evaluation of a Palato-Pharyngeal Implant System (PPIS) Obstructive Sleep Apnea Syndrome (OSAS)	N/A
Completed	`NCT03333876` - In Home Assessment of Three Anti-Snoring Devices, a Cross Over Study	N/A
Not yet recruiting	`NCT04143022` - Evaluation of the Effects of Acupuncture Press Needle in Mild to Moderate Obstructive Sleep Apnea Patients	N/A
Completed	`NCT02834767` - Genioglossus Muscle Training for Snoring and Obstructive Sleep Apnea	N/A
Withdrawn	`NCT01680380` - Tracking Breathing During Sleep With Non-contact Sensors	N/A
Terminated	`NCT01772017` - A Trial to Evaluate a Device for the Treatment of OSA and Snoring	N/A
Unknown status	`NCT00806637` - Vessel Sealing System Uvulopalatoplasty Versus Uvulopalatal Flap	N/A
Completed	`NCT00560859` - Childhood Adenotonsillectomy Study for Children With OSAS	N/A
Active, not recruiting	`NCT05643352` - Barbed Reposition Pharyngoplasty in Patients Complaining of Unilevel Palatal Snoring	N/A
Recruiting	`NCT05756647` - Mandibular Advancement vs Home Treatment for Primary Snoring	Phase 2
Completed	`NCT04086407` - Apnea Hypopnea Index Severity Versus Head Position During Sleep	N/A
Not yet recruiting	`NCT05116657` - Obstructive Sleep Apnoea Post Covid 19: Role of the Upper Airway Microbiome
Completed	`NCT01491828` - Study to Determine Results of Vibratory Stimulus on Subject's Neck	Phase 1
Completed	`NCT01322334` - Singing Exercises to Improve Symptoms of Snoring and Sleep Apnea	N/A
Terminated	`NCT03316963` - Neostigmine For Snoring During DISE	Early Phase 1
Completed	`NCT04063917` - Safety, and Tolerability of the ZENS Device (PLUTO)	N/A