At a glance
ClinicalIndex Comparison RecordN/ACompleted· 18 enrolled
Drug / intervention
Facial-Flexdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Facial-Flex as a Treatment for Snoring
In Brief
A clinical study evaluating Facial-Flex for Primary Snoring and Sleep Apnea. Completed, enrolled 18 participants across 1 site.
Detailed Summary
The study will test the hypothesis that training with the Facial-Flex exercise device for six weeks will improve snoring in patients with primary snoring or very mild sleep apnea.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPrimary Snoring, Sleep Apnea
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
201220132014201520162017201820192020202120222023202420252026
Enrollment StartFeb 2012
First PostedMar 2012
Primary CompletionDec 2012
TodayJul 2026
First PostedMar 15, 2012
Enrollment StartFeb 1, 2012
Primary CompletionDec 1, 2012
TodayJul 2, 2026
Enrollment to primary: 10 monthsPosted 14.3 years ago
Interventions
Facial-Flexdevice
Oral exercise device