Post Approval Study of the remedē System
NCT03425188 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 53
Last updated 2021-04-22
Summary
Prospective, single arm cohort study to evaluate the long-term safety, long-term effectiveness, and survival rate in subjects implanted with the remedē System.
Conditions
- Central Sleep Apnea
Sponsors & Collaborators
-
Respicardia, Inc.
lead INDUSTRY
Principal Investigators
-
Robin Germany, MD · Respicardia, Inc.
Eligibility
- Min Age
- 21 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2018-06-28
- Primary Completion
- 2020-08-04
- Completion
- 2020-08-04
Countries
- United States
- Germany
Study Locations
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