Snoring Clinical Trial
Official title:
Pilot Study to Assess the Effectiveness and Safety of Continuous Negative External Pressure (cNEP) in Reducing Respiratory Sounds in Individuals With Chronic Snoring
NCT number | NCT02767843 |
Other study ID # | SOM-011 |
Secondary ID | |
Status | Terminated |
Phase | N/A |
First received | |
Last updated | |
Start date | May 2016 |
Est. completion date | December 2016 |
Verified date | April 2024 |
Source | Sommetrics, Inc. |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This pilot study will examine the efficacy and safety of continuous negative external pressure ("cNEP") for the treatment of chronic snoring in people without obstructive sleep apnea.
Status | Terminated |
Enrollment | 4 |
Est. completion date | December 2016 |
Est. primary completion date | November 2016 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 70 Years |
Eligibility | Inclusion Criteria: - sleep test within the previous six months that shows snoring of at least 30 dB for at least 30% of total sleep time - AHI < 10/hr Exclusion Criteria: - previous neck surgery or radiation - carotid artery disease - serious medical or psychiatric illness - pregnancy - silicone allergy - excessive use of alcohol or sedating drugs |
Country | Name | City | State |
---|---|---|---|
United States | California Center for Sleep Disorders | Alameda | California |
Lead Sponsor | Collaborator |
---|---|
Sommetrics, Inc. |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Response | snoring decreased by <50% from baseline | one night | |
Primary | Adverse Events | all adverse events | one night | |
Secondary | Complete Response | snoring for < 5% of total sleep tim | one night |
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 |
NCT03333876 -
In Home Assessment of Three Anti-Snoring Devices, a Cross Over Study
|
N/A | |
Completed |
NCT03640793 -
Prospective Evaluation of a Palato-Pharyngeal Implant System (PPIS) Obstructive Sleep Apnea Syndrome (OSAS)
|
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 | |
Terminated |
NCT01772017 -
A Trial to Evaluate a Device for the Treatment of OSA and Snoring
|
N/A | |
Withdrawn |
NCT01680380 -
Tracking Breathing During Sleep With Non-contact Sensors
|
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 | |
Terminated |
NCT03701165 -
The Effect of the DryMouth Shield on Snoring
|
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 |