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Heart FailureMORE-CARENCT00885677

MOnitoring REsynchronization deviCes and cARdiac patiEnts

A study testing Medtronic CareLink® Network in people with Heart Failure, run by Medtronic Cardiac Rhythm and Heart Failure at 64 sites in 10 countries.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
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Trial 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. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Heart Failure
What is being tested?
Medtronic CareLink® Network
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
918 participants
Where
64 sitesin 10 countries
Study dates
Jun 2009to Jan 2016
Phase
Interventional
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • 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.
Show all 10Show fewer
  • 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.

Who cannot join

  • 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.
Show all 10Show fewer
  • Patient meets any exclusion criteria required by local law.
  • Inability or refusal to sign a patient informed consent form.
  • Patient's life expectancy is less than one year in the opinion of the physician
  • Patient is pregnant or breastfeeding.

Trial locations and contacts

64 sites in 10 countries.

64 sites in 10 countries

Italy29 sites
  • Policlinico Universitario

    Bari

  • Cliniche Gavazzeni

    Bergamo

  • Ospedali Riuniti

    Bergamo

  • Policlinico Universitario S. Orsola-Malpighi

    Bologna

  • Fondazione Poliambulanza

    Brescia

  • Ospedale V.E. Ferrarotto

    Catania

  • Ospedale Pugliese e Ciaccio

    Catanzaro

  • Sant'Anna Hospital

    Catanzaro

  • Ospedale Civile

    Chioggia, Venezia

  • Ospedale Unico della Versilia

    Lido Di Camaiore (LU)

  • Centro Cardiologico Monzino

    Milan

  • Ospedale San Paolo

    Milan

  • Ospedale Civile

    Mirano, Venezia

  • A.O. Monaldi

    Naples

  • Azienda Ospedaliera Sacro Cuore Don Calabria

    Negrar

  • Ospedale Giovan Battista Grassi

    Ostia Antica

  • Clinica San Carlo

    Paderno Dugnano

  • Ospedali Civico e Benfratelli

    Palermo

  • Ospedale San Salvatore

    Pesaro

  • Istituto di Fisiologia Clinica - CNR

    Pisa

  • Ospedale Santa Maria delle Croci

    Ravenna

  • Azienda Complesso Ospedaliero San Filippo Neri

    Roma

  • Policlinico Tor Vergata

    Roma

  • Policlinico Umberto I

    Roma

  • Ospedale Santa Maria Del Carmine

    Rovereto

  • P.O. di Trento P.O.S.Chiara

    Trento

  • Azienda Ospedaliera-Ospedali Riuniti

    Trieste

  • Ospedale E. Macchi

    Varese

  • Ospedale Civile Maggiore di Borgo Trento

    Verona

Other trials in Italy

France12 sites
  • Centre Hospitalier Universitaire de Angers

    Angers

  • Hôpital Cardiologique du Haut Lévêque

    Bordeaux

  • Centre Hospitalier

    La Rochelle

  • Hopital Louis Pradel

    Lyon

  • Hopital Saint Joseph

    Marseille

  • Hopital Arnaud de Villeneuve

    Montpellier

  • CHU

    Narbonne

  • Hopital La Source

    Orléans

  • Hopital La Pitie Salpetriere

    Paris, 75651

  • Clinique Bizet

    Paris

  • Hopital du Nord

    Saint-Etienne

  • CHRU

    Tours

Other trials in France

Spain7 sites
  • Hospital De Torrevieja

    Alicante

  • Hospital Reina Sofia

    Córdoba

  • Hospital Insular de Gran Canaria

    Las Palmas de Gran Canaria

  • Hospital Universitario de Valme

    Seville

  • Hospital General Universitario

    Valencia

  • Hospital Universitario La Fé

    Valencia

  • Complejo Hospitalario Universitario de Vigo

    Vigo

Other trials in Spain

Greece5 sites
  • Evaggelismos Hospital

    Athens, 10676

  • Henry Dynant Hospital - Athens

    Athens, 11526

  • University Hospital Herakleion

    Heraklion

  • HYGEIA - Hospital

    Marousi

  • University Hospital AHEPA Thessaloniki

    Thessaloniki, 54636

Other trials in Greece

Switzerland4 sites
  • Universitätsspital

    Basel

  • University Hospital

    Geneva

  • Kantonsspital St. Gallen

    Sankt Gallen

  • Triemli Hospital

    Zurich

Other trials in Switzerland

Hungary2 sites
  • Gottsegen György Országos Kardiológia Intézet GOKI

    Budapest

  • Semmelweis University AOK

    Budapest

Other trials in Hungary

Slovakia2 sites
  • NUSCH

    Bratislava

  • VUSCH

    Košice

Other trials in Slovakia

Czechia1 site
  • Institut Klinicke a Experimentalni Mediciny

    Prague

Other trials in Czechia

Israel1 site
  • Wolfson Medical Center

    Holon

Other trials in Israel

Netherlands1 site
  • MC Haaglanden - Locatie Westeinde

    The Hague

Other trials in Netherlands

About this study

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.
Read the 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.
Conditions
Heart Failure
Being tested
Medtronic CareLink® Network
Medical subject headings
Heart Failure

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Medtronic CareLink® NetworkDevice

    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.

Study groups in NCT00885677
Study groupRoleWhat they receive
Study GroupActive comparatorPatients 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.
Receives: Device: Medtronic CareLink® Network
Control GroupNo interventionPatients are CRT-D patients managed according to current standard clinical practice, based on routinely performed in-office visits.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. 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

    Measured: 1 year since the randomization

  2. 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

    Measured: 2 years after randomization

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Apr 2009 (estimated)
  2. Study startJun 2009
  3. Primary completionDec 2015
  4. Study completionJan 2016

Why it stopped: Low enrollment rate

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
918 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00885677
Sponsor's protocol ID
MDT-MORE-CARE
Acronym
MORE-CARE
Status last verified
Feb 2017
First submitted
21 Apr 2009
Last updated
2 Jul 2025
Data monitoring committee
Yes

Publications

  • Burri H, Quesada A, Ricci RP, Boriani G, Davinelli M, Favale S, Da Costa A, Kautzner J, Moser R, Navarro X, Santini M. The MOnitoring Resynchronization dEvices and CARdiac patiEnts (MORE-CARE) study: rationale and design. Am Heart J. 2010 Jul;160(1):42-8. doi: 10.1016/j.ahj.2010.04.005.

    PubMed 20598971
  • Boriani G, Da Costa A, Ricci RP, Quesada A, Favale S, Iacopino S, Romeo F, Risi A, Mangoni di S Stefano L, Navarro X, Biffi M, Santini M, Burri H; MORE-CARE Investigators. The MOnitoring Resynchronization dEvices and CARdiac patiEnts (MORE-CARE) randomized controlled trial: phase 1 results on dynamics of early intervention with remote monitoring. J Med Internet Res. 2013 Aug 21;15(8):e167. doi: 10.2196/jmir.2608.

    PubMed 23965236
  • Burri H, da Costa A, Quesada A, Ricci RP, Favale S, Clementy N, Boscolo G, Villalobos FS, Mangoni di S Stefano L, Sharma V, Boriani G; MORE-CARE Investigators. Risk stratification of cardiovascular and heart failure hospitalizations using integrated device diagnostics in patients with a cardiac resynchronization therapy defibrillator. Europace. 2018 May 1;20(5):e69-e77. doi: 10.1093/europace/eux206.

    PubMed 28679168
  • Boriani G, Da Costa A, Quesada A, Ricci RP, Favale S, Boscolo G, Clementy N, Amori V, Mangoni di S Stefano L, Burri H; MORE-CARE Study Investigators. Effects of remote monitoring on clinical outcomes and use of healthcare resources in heart failure patients with biventricular defibrillators: results of the MORE-CARE multicentre randomized controlled trial. Eur J Heart Fail. 2017 Mar;19(3):416-425. doi: 10.1002/ejhf.626. Epub 2016 Aug 28.

    PubMed 27568392

Questions about this trial

What is this clinical trial studying?

A study testing Medtronic CareLink® Network in people with Heart Failure, run by Medtronic Cardiac Rhythm and Heart Failure at 64 sites in 10 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 10 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: stopped early, as of the sponsor's last update on 2 Jul 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 64 sites in Italy, France, Spain, Greece, Switzerland and 5 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Yes. Results are posted in the registry (first posted 4 Apr 2017). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Phase 1: Median Time Between Event Onset Time and Clinical Decision for Each Subject. (time frame: 1 year since the randomization). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT00885677, which also lists 4 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Jul 2025.

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