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Re-evaluation of Optimal Re-synchronisation Therapy in Patients With Chronic Heart Failure

Not Applicable
Terminated
Conditions
Chronic Heart Failure
Interventions
Procedure: CRT-D implantation
Procedure: CRT-P implantation
Registration Number
NCT03494933
Lead Sponsor
Helios Health Institute GmbH
Brief Summary

The objective of the study is to demonstrate that in patients with chronic heart failure who receive optimal medical treatment for this condition and have indication for Cardiac Resynchronisation Therapy, the implantation of a pacemaker (index group) is not inferior to defibrillator (control group) with respect to all-cause mortality.

Detailed Description

Heart failure is a leading cause of death, hospitalisation, impaired quality of life and health expenditure. Symptoms and survival can be significantly improved by implantation of a device for Cardiac Resynchronisation Therapy (CRT). CRT devices are available as biventricular pacemakers (CRT-P) or as significantly more complex and cost-intensive biventricular defibrillators (CRT-D).

In patients who have previously experienced a life-threatening arrhythmia, the choice of the CRT-D (and not the CRT-P) is imperative but these are a small minority of patients. For the vast majority of patients receiving CRT therapy, there is currently considerable uncertainty as to whether the defibrillator function is needed and whether its benefits outweigh its risks. The defibrillator function may protect patients from sudden cardiac death. On the other hand, device-associated complications such as device infections appear to be increased; furthermore the defibrillator comes along with specific adverse events, particularly inappropriate shocks. These shocks are common and not only traumatic to patients (potentially leading to post-traumatic stress syndrome, anxiety disorders and depression), they also are negatively associated with overall survival.

The objective of the trial is to demonstrate that in patients with chronic heart failure who receive optimal medical treatment for this condition and have indication for CRT, the implantation of a CRT-P (index group) is not inferior to CRT-D (control group) with respect to all-cause mortality. Patients with an indication for CRT will be randomised to CRT-P or CRT-D.

RESET-CRT is an event-driven trial with a planned number of randomised and treated patients of at least n=1,356 (maximum of 2,004) and of 361 primary endpoints within an estimated median follow-up period of about 29 to 40 months.

No investigational medical product is defined to be used within RESET-CRT since only the therapeutic strategy (CRT-D versus CRT-P) is a pre-defined study treatment and allocated by random group (Proof of Strategy Trial). The devices to be implanted will be decided by the treating physician on the basis of the situation of the individual study patient and in line with local policies in routine clinical care.

Duration of study period:

Enrolment of 1,356 patients is expected to be completed within 52 months after inclusion of the first patient, i.e., by 31 December 2022. With an overall annual event rate between 9.0% and 12.5%, 361 primary endpoints will have occurred within 9 to 20 months of randomisation of the last patient (between 30 September 2023 and 31 August 2024). Under these circumstances, the total study duration will be between 62 and 73 months.

The Steering Committee of the study might prolong the recruitment period, for instance by 12 months, in the event of an unexpected slower recruitment rate or an overall event rate \< 9.0% for the primary endpoint.

For individual patients, the expected median follow-up time is between 29 and 40 months, with a minimum between 9 and 20 months and a maximum between 61 and 72 months. Follow-up may be prolonged by 12 months in the event of a prolonged recruitment period.

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
959
Inclusion Criteria
  • Age ≥18 years.
  • Symptomatic chronic heart failure due to ischemic or non-ischemic cardiomyopathy with NYHA class II, III or ambulatory IV.
  • Reduced left ventricular ejection fraction ≤35% in transthoracic echocardiography (TTE) or cardiac magnetic resonance imaging (MRI) assessed verifiably within 4 weeks prior to or on the day of enrolment.
  • On Optimal Medical Therapy (OMT) for at least 3 months prior to enrolment.
  • Class I or IIa indication for implantation of a device for cardiac resynchronisation therapy (according to 2016 Guidelines of the European Society of Cardiology for the diagnosis and treatment of acute and chronic heart failure).
  • Signed informed consent.

Exclusion criteria:

  • Class I or IIa indication for implantation of an ICD for secondary prevention of sudden cardiac death and ventricular tachycardia (according to the 2015 Guidelines of the European Society of Cardiology for the management of patients with ven-tricular arrhythmias and the prevention of sudden cardiac death).
  • Violation of Instruction For Use of the selected device by at least one of the random group treatments.
  • Ventricular tachycardia induced in an electrophysiological study.
  • Carrying any implanted cardiac pacemaker, defibrillator or CRT device.
  • Unexplained syncope.
  • Hospitalised with unstable heart failure with NYHA class IV within 1 month prior to enrolment.
  • Acute coronary syndrome or cardiac revascularization therapy by coronary angioplasty or coronary artery bypass grafting within 6 weeks prior to enrolment.
  • Cardiac valve surgery or percutaneous cardiac valvular intervention such as transcatheter aortic valve replacement or transcatheter mitral valve repair performed within 3 months prior to enrolment.
  • Reversible non-ischemic cardiomyopathy such as acute viral myocarditis or discontinuation of alcohol in alcohol-induced heart disease.
  • On the waiting list for heart transplant.
  • Any disease that limits life expectancy to less than 2 years.
  • Severe chronic renal disease (GFR<15 ml/min and/or the need for dialysis)
  • Participation in another clinical trial, either within the past 3 months or still ongoing (participation in sub-studies connected to this trial and participation in observational studies permitted).
  • Previous participation in RESET-CRT.
  • Pregnant women or women of childbearing potential not on adequate birth control.
  • Drug abuse or clinically manifest alcohol abuse.
Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
CRT-D groupCRT-D implantationIntervention: CRT-D implantation
CRT-P groupCRT-P implantationIntervention: CRT-P implantation
Primary Outcome Measures
NameTimeMethod
Time from randomisation to the occurrence of all-cause deathRandomization to end of study (event-driven, expected about 9 to 20 months after last patient in)

Time from randomisation to the occurrence of all-cause death

Secondary Outcome Measures
NameTimeMethod
Time from randomisation to first composite of Major Adverse Cardiac Event (MACE)Randomization to end of study (event-driven, expected about 9 to 20 months after last patient in)

Time from randomisation to first composite of Major Adverse Cardiac Event (MACE)

Changes in quality of life (EQ-5D) comparing inclusion/enrolment with 12 and 24 monthsat baseline, 12 and 24 months after randomisation

Quality of life will be measured using the European Quality of life 5 Dimension (EQ5D) questionnaire including its visual-analogue scale (Scores range from 0-100 where 0 is the worst score).

Time from randomisation to death from cardiac causesRandomization to end of study (event-driven, expected about 9 to 20 months after last patient in)

Time from randomisation to death from cardiac causes

Time from randomisation to sudden cardiac deathRandomization to end of study (event-driven, expected about 9 to 20 months after last patient in)

Time from randomisation to sudden cardiac death

Time from randomisation to life-threatening arrhythmiasRandomization to end of study (event-driven, expected about 9 to 20 months after last patient in)

Time from randomisation to life-threatening arrhythmias

Time from randomisation to first hospitalisation for cardiovascular reasonsRandomization to end of study (event-driven, expected about 9 to 20 months after last patient in)

Time from randomisation to first hospitalisation for cardiovascular reasons

Nights spent in hospital for cardiovascular reasons per year of follow-upRandomization to end of study (event-driven, expected about 9 to 20 months after last patient in)

Number of nights spent in hospital is calculated as time difference in days from hospital discharge to hospital admission. All hospital stays are serious adverse event by definition and will be assessed by an independent Endpoint Review Committee. The Endpoint Review Committee will also evaluate if a hospital stay for cardiovascular reasons is given. Per year of follow-up refers to a calculated number related to total follow-up duration of each patient normalised to years of follow-up.

Number of hospital readmissions for cardiovascular reasons after randomisationRandomization to end of study (event-driven, expected about 9 to 20 months after last patient in)

Number of hospital readmissions for cardiovascular reasons after randomisation

Total cost of treatment as compound endpoint of MACEs, number of hospital days for cardiovascular reasons and ambulatory visits for cardiovascular reasonsRandomization to end of study (event-driven, expected about 9 to 20 months after last patient in)

otal cost of treatment as compound endpoint of MACEs, number of hospital days for cardiovascular reasons and ambulatory visits for cardiovascular reasons

Trial Locations

Locations (113)

Marienhaus Klinikum im Kreis Ahrweiler

🇩🇪

Bad Neuenahr-Ahrweiler, Germany

Zentralklinik Bad Berka

🇩🇪

Bad Berka, Germany

Universitäts-Herzzentrum

🇩🇪

Bad Krozingen, Germany

Charité Campus Virchow-Klinikum

🇩🇪

Berlin, Germany

Helios Klinikum Berlin-Buch

🇩🇪

Berlin, Germany

Vivantes Klinikum Spandau

🇩🇪

Berlin, Germany

Helios Klinikum Emil von Behring

🇩🇪

Berlin, Germany

Jüdisches Krankenhaus Berlin

🇩🇪

Berlin, Germany

Ev.-Luth. Diakonissenanstalt zu Flensburg

🇩🇪

Flensburg, Germany

Klinikum Bielefeld

🇩🇪

Bielefeld, Germany

Berufsgenossenschaftliches Universitätsklinikum Bergmannsheil

🇩🇪

Bochum, Germany

Contilia Herz- und Gefäßzentrum

🇩🇪

Essen, Germany

Augusta Kliniken Bochum

🇩🇪

Bochum, Germany

Herz Zentrum Westfalen - Knappschaftskrankenhaus Dortmund

🇩🇪

Dortmund, Germany

St.-Johannes-Hospital Dortmund

🇩🇪

Dortmund, Germany

Knappschaftskrankenhaus Bottrop

🇩🇪

Bottrop, Germany

Universitätsmedizin Greifswald

🇩🇪

Greifswald, Germany

Hermann-Josef-Krankenhaus Erkelenz

🇩🇪

Erkelenz, Germany

Universitätsklinikum Erlangen

🇩🇪

Erlangen, Germany

Klinikum Fulda

🇩🇪

Fulda, Germany

Universitätsklinikum Frankfurt

🇩🇪

Frankfurt am Main, Germany

Kreiskrankenhaus Freiberg

🇩🇪

Freiberg, Germany

Universitätsklinikum Halle (Saale)

🇩🇪

Halle (Saale), Germany

Helios Klinikum Gotha

🇩🇪

Gotha, Germany

Klinikum Gütersloh gGmbH

🇩🇪

Gütersloh, Germany

Universitätsklinikum Hamburg-Eppendorf (UKE)

🇩🇪

Hamburg, Germany

Krankenhaus Martha-Maria Halle-Dölau

🇩🇪

Halle (Saale), Germany

Helios St. Marienberg Klinik Helmstedt

🇩🇪

Helmstedt, Germany

Klinikum Ingolstadt

🇩🇪

Ingolstadt, Germany

Universitätsklinikum Jena

🇩🇪

Jena, Germany

Städtisches Krankenhaus Kiel

🇩🇪

Kiel, Germany

Herzzentrum Leipzig

🇩🇪

Leipzig, Germany

Klinikum Leverkusen

🇩🇪

Leverkusen, Germany

Johannes Wesling Klinikum Minden

🇩🇪

Minden, Germany

Westpfalz-Klinikum GmbH

🇩🇪

Kaiserslautern, Germany

St.-Marien-Hospital Lünen

🇩🇪

Lünen, Germany

Universitätsklinikum Schleswig-Holstein

🇩🇪

Lübeck, Germany

Ev. Krankenhaus Bethesda Mönchengladbach

🇩🇪

Mönchengladbach, Germany

St. Vincenz-Krankenhaus

🇩🇪

Paderborn, Germany

Klinikum Nürnberg Süd

🇩🇪

Nürnberg, Germany

Johanniter-Krankenhaus Genthin-Stendal

🇩🇪

Stendal, Germany

Krankenhaus der Barmherzigen Brüder Trier

🇩🇪

Trier, Germany

Klinikum Landkreis Tuttlingen

🇩🇪

Tuttlingen, Germany

Schwarzwald-Baar Klinikum

🇩🇪

Villingen-Schwenningen, Germany

Universitätsklinikum Würzburg

🇩🇪

Würzburg, Germany

Heinrich-Braun-Klinikum

🇩🇪

Zwickau, Germany

Immanuel Klinikum Bernau - Herzzentrum Brandenburg

🇩🇪

Bernau bei Berlin, Germany

Universitätsklinikum Bonn

🇩🇪

Bonn, Germany

Carl-Thiem-Klinikum

🇩🇪

Cottbus, Germany

Helios Amper-Klinikum Dachau

🇩🇪

Dachau, Germany

Praxisklinik Herz und Gefäße

🇩🇪

Dresden, Germany

Klinikum Lippe Detmold

🇩🇪

Detmold, Germany

UKGM - Universitätsklinikum Gießen

🇩🇪

Gießen, Germany

Asklepios Harzklinik Goslar

🇩🇪

Goslar, Germany

Universitätsmedizin Göttingen

🇩🇪

Göttingen, Germany

Evangelisches Krankenhaus Hagen-Haspe

🇩🇪

Hagen, Germany

Asklepios Kliniken Hamburg GmbH - Asklepios Klinikum Harburg

🇩🇪

Hamburg, Germany

Asklepios Kliniken Hamburg GmbH

🇩🇪

Hamburg, Germany

Medizinische Hochschule Hannover (MHH)

🇩🇪

Hannover, Germany

St. Marien-Hospital Hamm

🇩🇪

Hamm, Germany

Oberhavel Kliniken

🇩🇪

Hennigsdorf, Germany

B. Braun Ambulantes Herzzentrum Kassel

🇩🇪

Kassel, Germany

Universitätsklinikum Heidelberg

🇩🇪

Heidelberg, Germany

Städtisches Klinikum Karlsruhe

🇩🇪

Karlsruhe, Germany

St. Vinzenz-Hospital

🇩🇪

Köln, Germany

Krankenhaus Porz am Rhein

🇩🇪

Köln, Germany

Universitätsklinikum Leipzig

🇩🇪

Leipzig, Germany

Technische Universität München

🇩🇪

München, Germany

Klinikum Lüdenscheid

🇩🇪

Lüdenscheid, Germany

Kliniken Maria Hilf

🇩🇪

Mönchengladbach, Germany

Städtische Kliniken Mönchengladbach - Elisabeth-Krankenhaus Rheydt

🇩🇪

Mönchengladbach, Germany

Universitätsklinikum Münster

🇩🇪

Münster, Germany

Harzklinikum Dorothea Christiane Erxleben Klinikum Quedlinburg

🇩🇪

Quedlinburg, Germany

Aller-Weser-Klinik - Krankenhaus Verden

🇩🇪

Verden, Germany

Diakonie Klinikum Jung-Stilling

🇩🇪

Siegen, Germany

Helios Klinikum Siegburg

🇩🇪

Siegburg, Germany

Krankenhaus Maria-Hilf Stadtlohn Klinikum Westmünsterland

🇩🇪

Stadtlohn, Germany

Sophien- und Hufeland-Klinikum

🇩🇪

Weimar, Germany

REGIOMED-KLINIKEN Klinikum Coburg

🇩🇪

Coburg, Germany

Herzzentrum Dresden Universitätsklinik

🇩🇪

Dresden, Germany

Helios Klinikum Erfurt

🇩🇪

Erfurt, Germany

München Klinik Neuperlach

🇩🇪

München, Germany

Helios Klinikum Aue

🇩🇪

Aue, Germany

RHÖN-KLINIKUM Campus Bad Neustadt

🇩🇪

Bad Neustadt a.d. Saale, Germany

Segeberger Kliniken

🇩🇪

Bad Segeberg, Germany

Herz- und Diabeteszentrum NRW - Universitätsklinik der Ruhr-Universität Bochum

🇩🇪

Bad Oeynhausen, Germany

Sana Klinikum Lichtenberg

🇩🇪

Berlin, Germany

Maria-Hilf-Krankenhaus Bergheim

🇩🇪

Bergheim, Germany

Unfallkrankenhaus Berlin

🇩🇪

Berlin, Germany

Albertinen Herz- und Gefäßzentrum - Albertinen Krankenhaus

🇩🇪

Hamburg, Germany

Helios Klinikum Hildesheim

🇩🇪

Hildesheim, Germany

Universitätsklinikum des Saarlandes

🇩🇪

Homburg, Germany

Universitätsklinikum Schleswig-Holstein Campus Kiel

🇩🇪

Kiel, Germany

Katholisches Klinikum Koblenz - Montabaur

🇩🇪

Koblenz, Germany

Helios Klinikum Krefeld

🇩🇪

Krefeld, Germany

Herzzentrum Uniklinik Köln

🇩🇪

Köln, Germany

Cardio Centrum Ludwigburg

🇩🇪

Ludwigsburg, Germany

Universitätsklinikum Magdeburg

🇩🇪

Magdeburg, Germany

Klinik Augustinum

🇩🇪

München, Germany

LMU Klinikum

🇩🇪

München, Germany

Marienhaus Klinikum St. Elisabeth Neuwied

🇩🇪

Neuwied, Germany

Havelland Kliniken

🇩🇪

Nauen, Germany

Elblandklinikum Riesa

🇩🇪

Riesa, Germany

Helios Vogtland-Klinikum Plauen

🇩🇪

Plauen, Germany

Universitätsmedizin Rostock

🇩🇪

Rostock, Germany

Helios Kliniken Schwerin

🇩🇪

Schwerin, Germany

Asklepios Klinikum Uckermark

🇩🇪

Schwedt/Oder, Germany

Marien Kliniken

🇩🇪

Siegen, Germany

Universitätsklinikum Ulm

🇩🇪

Ulm, Germany

Robert-Bosch-Krankenhaus

🇩🇪

Stuttgart, Germany

Helios Klinikum Warburg GmbH

🇩🇪

Warburg, Germany

Helios Universitätsklinikum Wuppertal

🇩🇪

Wuppertal, Germany

Rems-Murr-Klinikum Winnenden

🇩🇪

Winnenden, Germany

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