Clinical Research Directory
Browse clinical research sites, groups, and studies.
Registry of Central Sleep Apnea Patients Undergoing remedē System Implant
Sponsor: Zoll Medical Corporation
Summary
The goal of this observational study is to collect information on the safety and performance of the remedē System in patients with central sleep apnea who are undergoing the remedē System implant procedure. The main question\[s\] it aims to answer \[is/are\]: What is the incidence of serious adverse events related to the remedē System implant procedure, device, or delivered therapy through 12 months post implant. Participants will complete 2 home sleep apnea tests and be asked about adverse events. All other data collected will be from standard of care visits.
Key Details
Gender
All
Age Range
22 Years - Any
Study Type
OBSERVATIONAL
Enrollment
300
Start Date
2027-03
Completion Date
2037-05
Last Updated
2026-10-30
Healthy Volunteers
No
Conditions
Interventions
Phrenic nerve stimulation
remede System