RCT of Implantable Defibrillators in Patients With Non Ischemic Cardiomyopathy, Scar and Severe Systolic Heart Failure (BRITISH)
Primary Purpose
Heart Failure
Status
Recruiting
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Implantable Cardioverter-Defibrillator (ICD) or Cardiac Resynchronisation Therapy Defibrillator (CRTD)
Sponsored by
About this trial
This is an interventional treatment trial for Heart Failure focused on measuring Cardiac Magnetic Resonance Imaging (CMR), Implantable Cardioverter Device, Implantable Loop Recorder, Left ventricular ejection fraction (LVEF), Myocardial scar
Eligibility Criteria
Inclusion Criteria:
- A diagnosis of NICM on contrast-enhanced cardiovascular magnetic resonance imaging
- LV scar on routine CMR (patient without scar can enter the registry)
- New York Heart Association (NYHA) Heart Failure (HF) functional class I-III and severely impaired left ventricular function (LVEF ≤ 35% on any imaging modality) after a minimum of 3 months of treatment with optimal medical therapy (OMT) as recommended by National Institute for Health and Care Excellence (NICE)
- Able and willing to provide informed consent
Exclusion Criteria:
- New York Heart Association (NYHA) HF functional class IV after 3 months of optimal medical therapy (OMT)
- Acute decompensated heart failure
- Previous implantable device in situ (PPM, Cardiac Resynchronisation Therapy (CRT) or ICD)
- Ischemic cardiomyopathy (ICM) is defined as segmental wall motion abnormalities or wall thinning in a particular coronary territory with subendocardial or transmural late gadolinium enhancement (LGE). Patients with an LVEF ≤35% and a small amount of ischemic LGE (i.e. an infarct out of keeping with the amount of LV dysfunction) will not be excluded (so-called dual pathology patients)
- Known diagnosis of amyloidosis, sarcoidosis, arrhythmogenic right ventricular cardiomyopathy, or hypertrophic cardiomyopathy (diseases in which there are specific guidelines regarding defibrillator therapy)
- Known Lamin gene mutation or a positive family history of a Lamin gene mutation
- Valve disease is considered likely to require surgery during the 3 years follow-up period
- Complex congenital heart disease
- Any secondary prevention ICD indication
- Heart transplant recipient or admitted for cardiac transplantation/ left ventricular assist device
- Clinically apparent myocardial ischemia which requires revascularization
- Intracardiac mass which requires surgery
- Active endocarditis
- Active Septicaemia
- Pregnancy
- Life expectancy <2 years secondary to any other cause (i.e. malignancy)
- Active treatment with chemotherapy
- Severe renal failure (GFR <30)
- Actively participating in another study without prior agreement between both Chief Investigators
Sites / Locations
- Royal Bournemouth HospitalRecruiting
- Essex Cardiothoracic CentreRecruiting
- Portsmouth Hospitals University NHS TrustRecruiting
- Southampton Clinical Trials Unit
- University Hospital Southampton NHS Foundation TrustRecruiting
- Kent & Canterbury HospitalRecruiting
- Liverpool Heart & ChestRecruiting
- Glenfield HospitalRecruiting
- Wansbeck General HospitalRecruiting
- Aberdeen Royal InfirmaryRecruiting
- Royal Infirmary of EdinburghRecruiting
- New Cross HospitalRecruiting
- Leeds General InfirmaryRecruiting
- Pinderfields HospitalRecruiting
- St Bartholomew's HospitalRecruiting
- Guy's HospitalRecruiting
- Morriston HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
No Intervention
No Intervention
Arm Label
Intervention
Control
Registry
Arm Description
ICD or CRTD fitted
No ICD fitted (with Implantable Loop Recorder) or Cardiac Resynchronisation Therapy Pacemaker (CRTP)
Usual medical care
Outcomes
Primary Outcome Measures
Percentage of patients alive
All-cause mortality
Secondary Outcome Measures
Change in health-related quality of life measured using KCCQ-12
Short questionnaire including questions related to heart failure symptoms and how they affect daily activities
Change in health-related quality of life measured using EQ-5D-5L
Questionnaire consisting of 5 questions to evaluate a patients quality of life
Cardiovascular Death
Percentage of patients that have cardiovascular death
Sudden cardiac death
Percentage of patients that have sudden cardiac death
Aborted sudden cardiac death
Percentage of patients that have aborted sudden cardiac death
Appropriate ICD Therapy
Percentage of patients that have appropriate ICD therapy
Inappropriate ICD Therapy
Percentage of patients that have inappropriate ICD therapy
Significant ventricular arrhythmias
Percentage of patients that have significant ventricular arrhythmias
NYHA Status
Percentage of patients in each category
Heart failure hospitalisations
Number of events
Cardiac hospitalisations
Number of events
Procedures related to implanted device
Number of events
Percentage of patients alive
Mortality
Full Information
NCT ID
NCT05568069
First Posted
September 27, 2022
Last Updated
August 2, 2023
Sponsor
University Hospital Southampton NHS Foundation Trust
Collaborators
British Heart Foundation, University of Southampton
1. Study Identification
Unique Protocol Identification Number
NCT05568069
Brief Title
RCT of Implantable Defibrillators in Patients With Non Ischemic Cardiomyopathy, Scar and Severe Systolic Heart Failure
Acronym
BRITISH
Official Title
Using Cardiovascular Magnetic Resonance Identified Scar as the Benchmark Risk Indication Tool for Implantable Cardioverter Defibrillators in Patients With Non-Ischemic Cardiomyopathy and Severe Systolic Heart Failure
Study Type
Interventional
2. Study Status
Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
April 12, 2023 (Actual)
Primary Completion Date
April 1, 2026 (Anticipated)
Study Completion Date
April 1, 2036 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital Southampton NHS Foundation Trust
Collaborators
British Heart Foundation, University of Southampton
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
BRITISH is a UK multicentre trial of patients who have been diagnosed with heart failure due to Non-Ischemic Cardiomyopathy (NICM, or heart failure that is not caused by blocked heart arteries. Participants will be randomised into two groups. Half the participants will receive an Implantable Cardioverter-Defibrillator (ICD) and the other half will not. The aim of the study will be to compare all-cause mortality (death from any cause) between these two groups at 36 months, and longer-term to 10 years. The study has the potential to change international heart failure treatment guidelines and to improve how patients with this condition are managed.
Detailed Description
Patients with Non-Ischemic Cardiomyopathy (NICM) have a higher risk of experiencing serious abnormal heart rhythms that might be life-threatening. Current guidelines recommend fitting a device that can correct these serious heart rhythms (Implantable Cardioverter-Defibrillator (ICD)). However, research studies have shown that 90% of patients who have an ICD will never use it because they won't experience any serious heart rhythms. A recent large trial (DANISH) of over one thousand patients with severe Non-Ischemic Cardiomyopathy has called the current guidelines into question. The trial concluded that for patients who received an ICD, there was no difference in the likelihood of dying when compared to patients that didn't have an ICD fitted. As a result, many doctors are choosing not to implant an ICD in patients with this type of heart failure, as they believe there is no overall survival benefit. However, there are clues that some patients with NICM may still benefit from an ICD, even though the headline results suggest they are not necessary. It's likely that it's the patients who are at increased risk of having a serious abnormal heart rhythm that stand to benefit from ICDs. But having an ICD fitted carries with it a significant risk of problems developing e.g. bleeding, infection, lead problems, and inappropriate shocks. These risks may not outweigh the benefits and it is this question which BRITISH will address. The study will randomly assign (like the toss of a coin), half the study participants to receive an ICD and the other half to no ICD.
Both groups will be followed up to decide whether having an ICD fitted reduces the chances of dying.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure
Keywords
Cardiac Magnetic Resonance Imaging (CMR), Implantable Cardioverter Device, Implantable Loop Recorder, Left ventricular ejection fraction (LVEF), Myocardial scar
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Eligible patients will be randomised in a controlled fashion into two arms (n=1252):
Arm A: ICD implantation Arm B: No ICD implantation Patients with no scar on CMR will be followed up in a registry (n=1252)
Masking
None (Open Label)
Allocation
Randomized
Enrollment
2504 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Intervention
Arm Type
Experimental
Arm Description
ICD or CRTD fitted
Arm Title
Control
Arm Type
No Intervention
Arm Description
No ICD fitted (with Implantable Loop Recorder) or Cardiac Resynchronisation Therapy Pacemaker (CRTP)
Arm Title
Registry
Arm Type
No Intervention
Arm Description
Usual medical care
Intervention Type
Device
Intervention Name(s)
Implantable Cardioverter-Defibrillator (ICD) or Cardiac Resynchronisation Therapy Defibrillator (CRTD)
Intervention Description
An ICD is a device that is implanted under the skin under a local anesthetic. It has a battery/generator component and leads which are fixed into the heart chambers. It has the ability to detect dangerous heart rhythms if they occur, and deliver a shock to treat this to help prevent sudden cardiac death. A CRTD is a pacemaker with a defibrillator function.
Primary Outcome Measure Information:
Title
Percentage of patients alive
Description
All-cause mortality
Time Frame
3 years
Secondary Outcome Measure Information:
Title
Change in health-related quality of life measured using KCCQ-12
Description
Short questionnaire including questions related to heart failure symptoms and how they affect daily activities
Time Frame
3 years
Title
Change in health-related quality of life measured using EQ-5D-5L
Description
Questionnaire consisting of 5 questions to evaluate a patients quality of life
Time Frame
3 years
Title
Cardiovascular Death
Description
Percentage of patients that have cardiovascular death
Time Frame
3 years
Title
Sudden cardiac death
Description
Percentage of patients that have sudden cardiac death
Time Frame
3 years
Title
Aborted sudden cardiac death
Description
Percentage of patients that have aborted sudden cardiac death
Time Frame
3 years
Title
Appropriate ICD Therapy
Description
Percentage of patients that have appropriate ICD therapy
Time Frame
3 years
Title
Inappropriate ICD Therapy
Description
Percentage of patients that have inappropriate ICD therapy
Time Frame
3 years
Title
Significant ventricular arrhythmias
Description
Percentage of patients that have significant ventricular arrhythmias
Time Frame
3 years
Title
NYHA Status
Description
Percentage of patients in each category
Time Frame
3 years
Title
Heart failure hospitalisations
Description
Number of events
Time Frame
3 years
Title
Cardiac hospitalisations
Description
Number of events
Time Frame
3 years
Title
Procedures related to implanted device
Description
Number of events
Time Frame
3 years
Title
Percentage of patients alive
Description
Mortality
Time Frame
At 5 and 10 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
A diagnosis of NICM on contrast-enhanced cardiovascular magnetic resonance imaging
LV scar on routine CMR (patient without scar can enter the registry)
New York Heart Association (NYHA) Heart Failure (HF) functional class I-III and severely impaired left ventricular function (LVEF ≤ 35% on any imaging modality) after a minimum of 3 months of treatment with optimal medical therapy (OMT) as recommended by National Institute for Health and Care Excellence (NICE)
Able and willing to provide informed consent
Exclusion Criteria:
New York Heart Association (NYHA) HF functional class IV after 3 months of optimal medical therapy (OMT)
Acute decompensated heart failure
Previous implantable device in situ (PPM, Cardiac Resynchronisation Therapy (CRT) or ICD)
Ischemic cardiomyopathy (ICM) is defined as segmental wall motion abnormalities or wall thinning in a particular coronary territory with subendocardial or transmural late gadolinium enhancement (LGE). Patients with an LVEF ≤35% and a small amount of ischemic LGE (i.e. an infarct out of keeping with the amount of LV dysfunction) will not be excluded (so-called dual pathology patients)
Known diagnosis of amyloidosis, sarcoidosis, arrhythmogenic right ventricular cardiomyopathy, or hypertrophic cardiomyopathy (diseases in which there are specific guidelines regarding defibrillator therapy)
Known Lamin gene mutation or a positive family history of a Lamin gene mutation
Valve disease is considered likely to require surgery during the 3 years follow-up period
Complex congenital heart disease
Any secondary prevention ICD indication
Heart transplant recipient or admitted for cardiac transplantation/ left ventricular assist device
Clinically apparent myocardial ischemia which requires revascularization
Intracardiac mass which requires surgery
Active endocarditis
Active Septicaemia
Pregnancy
Life expectancy <2 years secondary to any other cause (i.e. malignancy)
Active treatment with chemotherapy
Severe renal failure (GFR <30)
Actively participating in another study without prior agreement between both Chief Investigators
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Zina Eminton
Phone
023 8026 8125
Email
z.b.eminton@soton.ac.uk
First Name & Middle Initial & Last Name or Official Title & Degree
Zoe Nicholas
Phone
023 8120 8538
Email
zoe.nicholas@uhs.nhs.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andrew Flett
Organizational Affiliation
University Hospital Southampton NHS Foundation Trust
Official's Role
Study Chair
Facility Information:
Facility Name
Royal Bournemouth Hospital
City
Bournemouth
State/Province
Dorset
ZIP/Postal Code
BH7 7DW
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Chris Critoph
Phone
01202 303626
Facility Name
Essex Cardiothoracic Centre
City
Basildon
State/Province
Essex
ZIP/Postal Code
SS16 5NL
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jason Dungu
Phone
01268 524900
Facility Name
Portsmouth Hospitals University NHS Trust
City
Portsmouth
State/Province
Hampshire
ZIP/Postal Code
PO6 3LY
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Geraint Morton
Phone
02392286000
Facility Name
Southampton Clinical Trials Unit
City
Southampton
State/Province
Hampshire
ZIP/Postal Code
SO16 6YD
Country
United Kingdom
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jacqui Nuttall
Phone
023 8120 3866
Email
J.Nuttall@soton.ac.uk
First Name & Middle Initial & Last Name & Degree
Zina Eminton
Phone
023 8026 8125
Email
Z.B.Eminton@soton.ac.uk
First Name & Middle Initial & Last Name & Degree
Andrew Flett, BSc, MBBS, FRCP, MD(Res)
First Name & Middle Initial & Last Name & Degree
Nick Curzen, BM(Hons) PhD FRCP
Facility Name
University Hospital Southampton NHS Foundation Trust
City
Southampton
State/Province
Hampshire
ZIP/Postal Code
SO16 6YD
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Andrew Flett
Phone
+44 (0)23 8120 8538
Email
andrew.flett@uhs.nhs.uk
First Name & Middle Initial & Last Name & Degree
Zoe Nicholas
Phone
+44 (0)23 8120 8538
Email
zoe.nicholas@uhs.nhs.uk
Facility Name
Kent & Canterbury Hospital
City
Canterbury
State/Province
Kent
ZIP/Postal Code
CT1 3NG
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Steven White
Phone
01227 766877
Facility Name
Liverpool Heart & Chest
City
Liverpool
State/Province
Lancashire
ZIP/Postal Code
L14 3PE
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Archie Rao
Phone
0151 600 1616
Facility Name
Glenfield Hospital
City
Leicester
State/Province
Leicestershire
ZIP/Postal Code
LE3 9QP
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gerry McCann
Phone
01268 524900
Facility Name
Wansbeck General Hospital
City
Ashington
State/Province
Northumbria
ZIP/Postal Code
NE63 9JJ
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
David Ripley
Phone
0344 811 8111
Facility Name
Aberdeen Royal Infirmary
City
Aberdeen
State/Province
Scotland
ZIP/Postal Code
AB25 2ZN
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dana Dawson
Phone
03454566000
Facility Name
Royal Infirmary of Edinburgh
City
Edinburgh
State/Province
Scotland
ZIP/Postal Code
EH16 4SA
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marc Dweck
Phone
0131 536 1000
Facility Name
New Cross Hospital
City
Wolverhampton
State/Province
West Midlands
ZIP/Postal Code
WV10 0QP
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anita Arya
Phone
01902 307999
Facility Name
Leeds General Infirmary
City
Leeds
State/Province
West Yorkshire
ZIP/Postal Code
LS1 3EX
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
John Greenwood
Phone
01132432799
Facility Name
Pinderfields Hospital
City
Wakefield
State/Province
West Yorkshire
ZIP/Postal Code
WF1 4DG
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Peter Swaboda
Phone
01924 541000
Facility Name
St Bartholomew's Hospital
City
London
ZIP/Postal Code
EC1A 7BE
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kostas Savvatis
Phone
0207 3777 000
Facility Name
Guy's Hospital
City
London
ZIP/Postal Code
SE1 9RT
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anoop Shetty
Phone
020 7188 7188
Facility Name
Morriston Hospital
City
Swansea
ZIP/Postal Code
SA6 6NL
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Geraint Jenkins
Phone
01792 702222
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
RCT of Implantable Defibrillators in Patients With Non Ischemic Cardiomyopathy, Scar and Severe Systolic Heart Failure
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