Clinical Trials Directory

Trials / Completed

CompletedNCT00490984

Tongue Advancement for Obstructive Sleep Apnea

Tongue Advancement for Obstructive Sleep Apnea. An Evaluation fo the Aspire Medical Advance System.

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Aspire Medical · Industry
Sex
All
Age
20 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The objective of this study is to assess the feasibility, safety and effectiveness of tongue stabilization using Aspire Medical Advance™ System for the treatment of obstructive sleep apnea (OSA). Success is defined as a statistically significant reduction in AHI measured by polysomnography (PSG) from baseline to 6 months.

Detailed description

Obstructive sleep apnea (OSA) is a major health problem in the United States and can result in excessive daytime sleepiness and cardiovascular problems. The primary treatment for OSA today is continuous positive airway pressure (CPAP). Many patients however are unable to tolerate sleeping with a CPAP machine. Surgery is one of the main treatment options available today to these CPAP-intolerant patients. However, current methods of sleep surgery are painful, morbid, and/or lack decent effectiveness. This trial will measure the effectiveness of the Advance System, an implantable medical device to treat OSA. In the trial, patients who meet the study entry criteria receive a baseline sleep study (PSG). The Advance System is then implanted and 6 months after implantation, another PSG is performed. The trial will compare the baseline and the 6 month apnea-hypopnea indices

Conditions

Interventions

TypeNameDescription
DEVICEAspire Medical Advance SystemThe treatment includes a device that is surgically implanted in the tongue and lower jaw. The purpose of the implant is to prevent obstruction of the upper airway thereby improving breathing during sleep.

Timeline

Start date
2006-02-01
Primary completion
2009-02-01
Completion
2009-07-01
First posted
2007-06-25
Last updated
2009-12-23

Locations

3 sites across 3 countries: Belgium, Czechia, Germany

Source: ClinicalTrials.gov record NCT00490984. Inclusion in this directory is not an endorsement.