Respiration Patterns With Impedance in LINQ (EPIQ)

Medtronic

Status

Completed

Conditions

Breathing Exercises

Treatments

Device: respiration assessment

Study type

Interventional

Funder types

Industry

Identifiers

NCT02828735

EPIQ

Details and patient eligibility

About

The purpose of the study is to evaluate the use of subcutaneous impedance measured with an implanted Medtronic Reveal LINQ™ insertable cardiac monitor (ICM) as respiratory rate monitor.

Enrollment

20 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Suspected arrhythmia Diastolic Heart Failure and/or in Renal Failure.
Chronic Kidney Disease (CKD) in Stage 5 (GFR = <15 mL/min).
Diastolic Heart Failure in class II and class III (class IV to be considered in end stage and non-reversible).
Willing to sign the informed consent form.
Greater than 18 years of age.

Exclusion criteria

Enrolled in another study that could confound the results of this study, without documented pre-approval from a Medtronic study manager.
Significant respiratory diseases such as COPD or pulmonary hypertension.
Frequent arrhythmias, including PVC's.
Known systolic heart failure.
Recent infection.
Allergenic or rejection reaction to materials used in incision/insertion tools, Reveal LINQ™ ICM exterior or incision closure method.
Active implanted cardiac medical device (e.g. IPG, ICD, CRT, etc).
Not suitable for Reveal LINQ™ implantation (e.g., severe cachexia, dermatologic conditions of the skin) or any concomitant condition which in the opinion of the investigator would not allow a safe participation in the study.
Body conditions that would complicate accurate measurement of respiratory efforts with an external device deployed around the chest.
Not able to take the postures as necessary for the study protocol and not able to walk continuously for a period of 6 minutes.
Any concomitant condition which in the opinion of the investigator would not allow a safe participation in the study.