At a glance
ClinicalIndex Comparison RecordN/ACompleted· 95 enrolled
Drug / intervention
Reza Band UES Assist Devicedevice
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.
A Multi-Center, Non-Randomized, Prospective Study of the Reza Band™ Upper Esophageal Sphincter (UES) Assist Device for the Treatment of Esophagopharyngeal Reflux
In Brief
A clinical study evaluating Reza Band UES Assist Device for Laryngopharyngeal Reflux. Completed, enrolled 95 participants across 5 sites.
Detailed Summary
The purpose of the study is to determine the safety and effectiveness of non-invasive Reza Band UES Assist Device for the treatment of esophagopharyngeal reflux with extra-esophageal symptoms (chronic cough, choking, aspiration, chronic post nasal drip, globus, sore throat, throat clearing).
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsLaryngopharyngeal Reflux
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
20132014201520162017201820192020202120222023202420252026
Enrollment StartApr 2013
First PostedMay 2013
Primary CompletionSep 2013
TodayJul 2026
First PostedMay 20, 2013
Enrollment StartApr 1, 2013
Primary CompletionSep 1, 2013
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 13.1 years ago
Interventions
Reza Band UES Assist Devicedevice
Device is worn by patient to reduce or eliminate laryngopharyngeal reflux