Heart Failure
Conditions
Keywords
Heart Failure
Brief summary
The purpose of this non-randomized, cross-over, unblinded, single-center feasibility study is to assess the sensitivity of the LINQ ICM to measure derived-subcutaneous impedance in patients with heart failure during periods when diuretics and/or HF-medication consumption is increased or suspended for 48 hours (up to 72 hours at physician discretion) and to collect safety information related to HF status and to medication consumption changes.
Detailed description
Up to 30 subjects with a clinical diagnosis of Heart Failure will be enrolled in the study. It is expected that the subjects will be enrolled over a period of approximately 6 months. 3 follow up visits are planned at 2, 4 and 6 months (+/- one week) following the LINQ ICM implant. The total expected duration of the study is of about 1 year. According to the enrolment chronological order, each subject will be allocated to Diuretic Suspension group (DS), Diuretic Increase (DI) or Diuretic+MRA medication Suspension (DMS), which will define the medication regimen before the follow-up visit. Primary objective of the study is detecting the variation of impedance magnitude and the time of occurrence after medication regimen changes will be evaluated at each follow-up.
Interventions
DRUGDiuretic Suspension (DS)
Stop diuretic consumption in the 48h before the follow-up visit
DRUGDiuretic Increase (DI)
Double diuretics dosage in the 48h before the follow-up visit
DRUGDiuretic and Medication Suspension (DMS)
Stop diuretic and MRA medication consumption in the 48h before the follow-up visit
Sponsors
Medtronic BRC
Study design
Allocation
NON_RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
NONE
Intervention model description
According to the enrolment chronological order, each subject will be allocated to Diuretic Suspension group (DS), Diuretic Increase (DI) or Diuretic+MRA medication Suspension (DMS), which will define the medication regimen before the follow-up visit.
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Clinical Diagnosis of Heart Failure * Plasma NT-proBNP (\>250ng/L in SR and \>1,000ng/L in AF) * LVEF \<50% measured in the year before enrolment * Treated routinely with a daily dose of loop diuretic * Receiving other guideline-indicated therapy for heart failure * Willing to sign the informed consent form. * Greater than 18 years of age.
Exclusion criteria
* Pregnant patients (all females of child-bearing potential must have a negative pregnancy test before LINQ ICM implant) * eGFR \<30 ml/minute. * Any concomitant condition which in the opinion of the investigator would not allow a safe participation in the study. * Patients with implanted pacemakers or defibrillators * Severe aortic or mitral valve disease * Breathlessness at rest or on minor exertion. * Chest pain at rest or on mild or moderate exertion. * Patients deemed too unstable to miss 48 hours of heart failure treatment * Enrolled in another study that could confound the results of this study, without documented pre-approval from Medtronic study manager
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Derived-subcutaneous impedance | 2 months | The variation of impedance magnitude and the time of occurrence after medication regimen changes will be detected by the LINQ ICM |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Number of Adverse Events | 6 months | All AEs related to changes in the therapeutic regimen and/or to HF status will be collected through CRF completion |
| Number of Transitory Arrhythmias | 6 months | Any transitory arrhythmias related to drug regimen changes and/or HF condition will be collected through CRF completion |
Countries
United Kingdom
Contacts
Primary ContactTeodora Bellone
Backup ContactMirko De Melis
Outcome results
None listed