This website uses cookies to enhance your browsing experience, improve site performance, and gather analytics. By selecting 'Accept,' you consent to these cookies as described in our Privacy Policy.

Reveal LINQ Respiration Clinical Study

Sponsored by Medtronic Cardiac Rhythm and Heart Failure

About this trial

Last updated 3 years ago

Study ID

MDT20022

Status

Completed

Type

Observational

Placebo

No

Accepting

18-75 Years
55+ Years
All
All

Trial Timing

Ended 4 years ago

What is this trial about?

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.

What are the participation requirements?

Yes

Inclusion Criteria

- 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

No

Exclusion Criteria

- 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

Locations

Location

Status