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MOnitoring REsynchronization deviCes and cARdiac patiEnts

MOnitoring REsynchronization deviCes and cARdiac patiEnts

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00885677
Acronym
MORE-CARE
Enrollment
918
Registered
2009-04-22
Start date
2009-06-30
Completion date
2016-01-31
Last updated
2025-07-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure

Brief summary

The objective of this study is to compare two different strategies of disease management in heart failure patients treated with cardiac resynchronization therapy devices 1. Remote monitoring with CareLink Network System 2. Standard management of the disease by means of scheduled routine in-patient follow-ups; and to demonstrate that the remote monitoring strategy is superior to the standard strategy, both in terms of clinical effectiveness and total healthcare system utilization.

Detailed description

Major cardiovascular adverse events in patients with heart failure treated with cardiac resynchronization therapy (CRT-D) represent a big concern to the medical community, as they require hospitalizations and may lead to death. Subjects with a history of heart failure are counseled regarding the importance of contacting their clinicians promptly if they experience any changes or worsening of their condition. Acute heart failure episodes with hospitalizations represent one of the most relevant causes of health status deterioration for these patients. Moreover, atrial arrhythmias occurrence is a big issue, as it increases the risk of heart failure itself, stroke and inappropriate shocks. In addition to affecting patient health, hospital admission resulting from these complications will impact healthcare costs. Latest generations of Medtronic CRT-D devices are equipped with a system that triggers an alarm if possible fluid accumulation is detected (OptiVol). This may initiate patient-clinician contact before evident cardiac decompensation. Moreover, advanced diagnostic capabilities for detecting atrial arrhythmias occurrence and total burden are available on such devices. Importantly, all these devices are now able to inform physician of these events by remote monitoring with CareLink Network parameters, and have the potential of playing a key role in patient monitoring. Over the last years, interest has been increasing in remote monitoring models for delivering care to HF patients, either as telemonitoring (transfer of physiological data through telephone or digital cable from home to healthcare provider) or as regular structured telephone contacts between patients and healthcare providers, which may or may not include data transfer. Several studies with relatively large numbers of patients have been published (see table). A recent meta-analysis found that remote monitoring programs for patients with chronic HF living in the community reduced admissions to hospital and all cause mortality by nearly one fifth while improving health related quality of life, but had no significant effect on all cause admission to hospital. However, none of the published studies considered remote monitoring systems able to provide device-detected information on fluid accumulation, AT/AF total burden, arrhythmias occurrence and device-related issues in patients treated with CRT-D devices. Early intervention may then be a key element in avoiding major cardiovascular events to occur and possible deterioration of the disease progression. The Carelink Network remote monitoring system, through Care Alerts, may initiate subject-clinician contact before typical signs and symptoms are exhibited, since it provides the physician with an automatic alert for atrial arrhythmias occurrence, fluid accumulation, and system integrity issues. However, clinical evidence must be provided of the superiority of this patient management strategy with respect to standard clinical practice, based on routine in-office visits. Very recent findings showed that the use of CareLink in European clinical practice is technically feasible and that remote follow-up is an efficient method of surveillance of implanted patients. Moreover, the early detection and review of device and clinical events suggest the potential impact of remote monitoring on overall patient care. There are a number of possible limitations with remote monitoring. The CareLink Network system requires that the patient establishes an initial contact between the device and the remote monitor unit, and that the unit is properly hooked up to the phone line. Not all patients may be able to perform the setup properly. There may be a delay by the physician in consulting patient data (for example over weekends), with a risk of adverse events occurring during that interval. There may be difficulties in contacting patients (e.g. if they are traveling). These possible limitations need to be properly assessed, especially for monitoring atrial arrhythmias, where the time factor is of importance for avoiding complications. Remote patients' disease management has the potential for avoiding hospitalization. Clear demonstration that remote monitoring of AT/AF/HF plus strict treatment guidelines leads to a reduction in hospitalization rates has not been proven, and it could be a major argument for using this technology in routine clinical practice. The MORE-CARE Study is aimed at comparing two different strategies of disease management in heart failure patients treated with CRT-D devices: 1. Remote disease management via Carelink Network system 2. Standard disease management by means of scheduled routine in-patient follow-ups. The main objective of the study is to demonstrate that the remote management strategy is superior to the standard strategy, both in terms of clinical effectiveness and total healthcare system utilization.

Interventions

Continuous monitoring via a disease remote management system. Patients of the Study group will receive a remote monitor and their device will be programmed to have wireless telemetry, Care Alerts, and the ability to transmit over the Medtronic CareLink® network. Clinical and device conditions will be then monitored continuously and alarms for the physician will be generated if a set of pre-defined potentially harming conditions should occur.

Sponsors

Medtronic Cardiac Rhythm and Heart Failure
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient indicated to CRT-ICD according to current guidelines: * Left ventricular systolic dysfunction (LVEF≤35%), * New York Heart Association functional class III-IV, * QRS≥120 ms * Optimized medical treatment. * Patient implanted within the last 8 weeks with Medtronic CRT-ICD device equipped with fluid accumulation diagnostics, AT/AF monitoring capability, wireless telemetry for automatic remote data transmission and alerting system for physician. * Patient with less than 8 weeks follow-up, who has not received Carelink® Network Monitor and was not managed by Cardiac Compass report reviewing. * Carelink Network is available at patient's home * Patient or the patient's caregiver is willing and able to use the Medtronic CareLink® Network Monitor and to perform the required duties at home or has a family member or assistant perform those duties. * Patient is willing and able to sign an informed consent form.

Exclusion criteria

* Inability to fully understand the instructions relating to remote monitoring using CareLink® Network. * Permanent AT/AF. * Patient had not been previously implanted with a CRT/CRT-D device. * Patient has medical conditions that would limit study participation. * Patient is less than 18 years of age. * Patient is enrolled in or intends to participate in another clinical trial that may have an impact on the study endpoints. * Patient meets any

Design outcomes

Primary

MeasureTime frameDescription
Phase 1: Median Time Between Event Onset Time and Clinical Decision for Each Subject.1 year since the randomizationThe median delay from device-detected events to clinical decisions was considerably shorter in the Remote group compared to the Control group
Phase 2: Combined Endpoint of Death From Any Cause, Cardiovascular and Device-related Hospitalizations (at Least 48 Hours Stay), Calculated as Number of Subjects With at Least One Event2 years after randomizationTime to first event

Countries

Czechia, France, Greece, Hungary, Israel, Italy, Netherlands, Slovakia, Spain, Switzerland

Participant flow

Recruitment details

918 patients have been enrolled in the study, from 29/05/2009 (date of first enrollment) until 20/08/2014 (date of last enrollment).

Pre-assignment details

918 subjects signed the Informed Consent Form. One of those subjects withdraw from the study prior randomization, therefore 917 subjects were randomized either to Study (462) or to Control (455) groups.

Participants by arm

ArmCount
Study Group
Patients of the study arm are CRT-D patients followed-up by means of a remote disease management system (Medtronic Carelink® Network), for which an automatic alerting system is enabled for fluid accumulation, AT/AF episodes and system integrity. Medtronic CareLink® Network: Continuous monitoring via a disease remote management system. Patients of the Study group will receive a remote monitor and their device will be programmed to have wireless telemetry, Care Alerts, and the ability to transmit over the Medtronic CareLink® network. Clinical and device conditions will be then monitored continuously and alarms for the physician will be generated if a set of pre-defined potentially harming conditions should occur.
437
Control Group
Patients are CRT-D patients managed according to current standard clinical practice, based on routinely performed in-office visits.
428
Total865

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyDeath4034
Overall Studydevice/lead revision or replacement76
Overall StudyHeart transplantation10
Overall StudyInclusion/exclusion not met2527
Overall StudyLost to Follow-up1513
Overall Studypremature study closure4144
Overall StudyProtocol Violation5454

Baseline characteristics

CharacteristicStudy GroupTotalControl Group
Age, Continuous66 years
STANDARD_DEVIATION 11
66 years
STANDARD_DEVIATION 10
67 years
STANDARD_DEVIATION 10
History of AF
History of AF
89 participants151 participants62 participants
History of AF
Missing
8 participants13 participants5 participants
History of AF
No History of AF
340 participants701 participants361 participants
History of Myocardial Infarction
Missing
11 participants14 participants3 participants
History of Myocardial Infarction
With History of Myocardial Infarction
164 participants337 participants173 participants
History of Myocardial Infarction
Without History of Myocardial Infarction
262 participants514 participants252 participants
LVEF27.3 %
STANDARD_DEVIATION 6.6
27.3 %
STANDARD_DEVIATION 6.3
27.4 %
STANDARD_DEVIATION 6
Region of Enrollment
France
85 participants162 participants77 participants
Region of Enrollment
Greece
21 participants40 participants19 participants
Region of Enrollment
Hungary
6 participants12 participants6 participants
Region of Enrollment
Israel
3 participants6 participants3 participants
Region of Enrollment
Italy
225 participants456 participants231 participants
Region of Enrollment
Netherlands
4 participants9 participants5 participants
Region of Enrollment
Slovakia
12 participants23 participants11 participants
Region of Enrollment
Spain
46 participants89 participants43 participants
Region of Enrollment
Switzerland
35 participants68 participants33 participants
Sex: Female, Male
Female
95 Participants211 Participants116 Participants
Sex: Female, Male
Male
342 Participants654 Participants312 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
68 / 46285 / 455
serious
Total, serious adverse events
184 / 462168 / 455

Outcome results

Primary

Phase 1: Median Time Between Event Onset Time and Clinical Decision for Each Subject.

The median delay from device-detected events to clinical decisions was considerably shorter in the Remote group compared to the Control group

Time frame: 1 year since the randomization

Population: Phase 1: A total of 154 patients were enrolled from May 2009 through April 2010 from 32 centers in 6 different countries (France, Hungary, Israel, Italy, Spain, and Switzerland). The final patient cohort object of analysis comprised 148 patients (76 in the Remote group and 72 in the Control group)

ArmMeasureValue (MEDIAN)
Study GroupPhase 1: Median Time Between Event Onset Time and Clinical Decision for Each Subject.2 days
Control GroupPhase 1: Median Time Between Event Onset Time and Clinical Decision for Each Subject.29 days
Primary

Phase 2: Combined Endpoint of Death From Any Cause, Cardiovascular and Device-related Hospitalizations (at Least 48 Hours Stay), Calculated as Number of Subjects With at Least One Event

Time to first event

Time frame: 2 years after randomization

Population: All subjects in analysis were included in the primary endpoint analysis

ArmMeasureValue (NUMBER)
Study GroupPhase 2: Combined Endpoint of Death From Any Cause, Cardiovascular and Device-related Hospitalizations (at Least 48 Hours Stay), Calculated as Number of Subjects With at Least One Event134 participants
Control GroupPhase 2: Combined Endpoint of Death From Any Cause, Cardiovascular and Device-related Hospitalizations (at Least 48 Hours Stay), Calculated as Number of Subjects With at Least One Event126 participants

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026