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OSPREY Study

Treating Obstructive Sleep Apnea using Targeted Hypoglossal Neurostimulation (The OSPREY Study)

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AGE: +22 years old
GENDER: All
HEALTHY PARTICIPANTS: No
TYPE: Interventional Treatment Study
CONDITION: Obstructive Sleep Apnea (OSA), Apnea+Hypopnea, Hypopnea, Sleep
LOCATION: University Hospitals Cleveland Medical Center

Learn More About This Research Study

For more information, please contact study coordinator, Xiuhua Yuan, at 216-844-2371 and leave a message or complete the online form below.

Study Purpose

The purpose of this research study is to demonstrate the safety and effectiveness of the aura6000® System after 6 months of stimulation therapy when compared to a control group with no stimulation, when used in patients with moderate to severe obstructive sleep apnea

Who Can Participate

Participants 22 years and older diagnosed with moderate to severe OSA may be eligible for this study.

Request More Information

Please complete the form below to be contacted by a study representative and learn more about this study.

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