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Treatment of Extraesophageal Reflux With the Reza Band UES Assist Device

NCT01857713 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 95

Last updated 2015-06-19

Study results available
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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).

Conditions

  • Laryngopharyngeal Reflux

Interventions

DEVICE

Reza Band UES Assist Device

Device is worn by patient to reduce or eliminate laryngopharyngeal reflux

Sponsors & Collaborators

  • Somna Therapeutics, L.L.C.

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-04-30
Primary Completion
2013-09-30
Completion
2013-09-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01857713 on ClinicalTrials.gov