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Magnetic Apnea Prevention(MAGNAP) Device to Treat Obstructive Sleep Apnea:First-In-Human Study of Feasibility and Safety — MAGNAP  

Obstructive Sleep Apnea Clinical Trial

Official title:
Magnetic Apnea Prevention (MAGNAP) Device to Treat Obstructive Sleep Apnea: First-In-Human Study of Feasibility and Safety

Clinical Trial Summary

The purpose of this study is to determine the safety and feasibility of the Magnap magnetic device in the treatment of obstructive sleep apnea (OSA).

Clinical Trial Description

Magnap is a magnet-activated treatment for obstructive sleep apnea (OSA) designed to be less invasive than reconstructive surgery, more tolerable than positive airway pressure, and more effective than non-invasive therapies for OSA. The Magnap device consists of a neodymium-iron-boron rare earth magnet with a ferromagnetic directional back-plate encased in titanium. The device will be implanted surgically on the hyoid bone. Following surgery, the patient is fitted with a custom, removable external neck accessory containing a second magnet, which is worn during sleep and prevents airway collapse by attracting the internal hyoid magnet with sufficient force to keep the airway open . ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02431507
Study type Interventional
Source University of California, San Francisco
Contact Kelcey Harrison, BA
Phone (415) 305-5974
Email Kelcey@magnap.net
Status Recruiting
Phase N/A
Start date September 2015
Completion date December 2024
View Details
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