remedē System Therapy Study

Running, not enrolling

Conditions studied: Central Sleep Apnea

In brief

The purpose of this non-randomized post market study is to collect clinical data on the safety and effectiveness of the remedē System in a real-world setting.

Key facts

Study ID
NCT03884660
Run by
Respicardia, Inc.
People needed
225
Starts
2019-06-18
Expected to finish
2030-12-30
Last updated by the study team
2025-07-24

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

Where it is running

Full record on ClinicalTrials.gov

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