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Janus II Feasibility
Sponsor: Zoll Medical Corporation
Summary
The objectives of this study are to evaluate the feasibility of the remedē® Dual Channel System at implant and overnight sleep studies and to assess chronic safety.
Official title: Janus II: A Feasibility Study to Evaluate Response to Remede Dual Channel System Therapy
Key Details
Gender
All
Age Range
22 Years - Any
Study Type
INTERVENTIONAL
Enrollment
40
Start Date
2025-08-12
Completion Date
2034-12
Last Updated
2025-10-29
Healthy Volunteers
No
Conditions
Interventions
Dual Channel Stimulation
implant of dual channel stimulation device
Locations (3)
The Insomnia and Sleep Institute of Arizona LLC
Scottsdale, Arizona, United States
The University of Michigan Health-West
Wyoming, Michigan, United States
The Ohio State University
Columbus, Ohio, United States