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RECRUITING
NCT06556693
NA

Janus II Feasibility

Sponsor: Zoll Medical Corporation

View on ClinicalTrials.gov

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

DEVICE

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