Sleep Medicine Research
OSPREY Study
Treating Obstructive Sleep Apnea using Targeted Hypoglossal Neurostimulation (The OSPREY Study)
AGE: +22 years old
GENDER: All
HEALTHY PARTICIPANTS: No
GENDER: All
HEALTHY PARTICIPANTS: No
TYPE: Interventional Treatment Study
CONDITION: Obstructive Sleep Apnea (OSA), Apnea+Hypopnea, Hypopnea, Sleep
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.
- STUDYID: SITE00001872
- NCT04950894