Reveal LINQ Respiration Clinical Study
Completed
Conditions studied: Respiratory Rate
In brief
The LINQ™ Respiration study will collect and characterize Reveal LINQ™ derived respiration data from patients undergoing a simulated 24-hour time period while being monitored with capnography.
Key facts
- Study ID
- NCT04506684
- Run by
- Medtronic Cardiac Rhythm and Heart Failure
- People needed
- 79
- Starts
- 2020-09-25
- Expected to finish
- 2021-07-31
- Last updated by the study team
- 2023-12-18
Who can join
Age: 55 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patient is ≥ 55 years old
- Patient (or patient's legally authorized representative) is willing and able to provide written informed consent
- Patient is willing and able to comply with the study procedures
- Patient has an active Medtronic Reveal LINQ device that has been implanted for ≥ 60 days and no more than 3 years
You may not qualify if…
- Patient has an existing condition that necessitates the use of supplemental oxygen
- Patient has an active acute respiratory infection or a respiratory disorder that may affect ability to perform respiratory maneuvers
- Patient has NYHA Class IV heart failure per most recent assessment
- Any concomitant condition that might endanger the patient through participation in the study or interfere with study procedures, as assessed by the investigator
- Patient is enrolled in another study that could confound the results of this study
- Patient has an existing implantation of Medtronic IPG, ICD, CRT-D or CRT-P device
Where it is running
- Cardiac Arrhythmia Service — Boca Raton, Florida, United States
- CentraCare Heart & Vascular Center — Saint Cloud, Minnesota, United States
- Oklahoma Heart Hospital Research Foundation — Oklahoma City, Oklahoma, United States
- The Stern Cardiovascular Foundation — Germantown, Tennessee, United States
Full record on ClinicalTrials.gov
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