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A Pilot Feasibility Study in Recovered Heart Failure (TRED)

Primary Purpose

Heart Failure

Status
Unknown status
Phase
Phase 4
Locations
United Kingdom
Study Type
Interventional
Intervention
Withdrawal of therapy
Sponsored by
Royal Brompton & Harefield NHS Foundation Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Heart Failure focused on measuring Recovery

Eligibility Criteria

16 Years - 85 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Have an index diagnosis of heart failure confirmed by 2 independent operators based on clinical details.
  2. Be currently taking at least 1 of the following medications loop diuretic, betablocker, angiotension converting enzyme inhibitor/angiotensin receptor blocker and mineralocorticoid receptor antagonist.
  3. Have demonstrated evidence of left ventricular reverse remodelling following the initial diagnosis with subsequent improvement in ejection fraction to >50% and normalisation of left ventricular (LV) volumes.
  4. Have no symptoms of heart failure (NYHA Class 1).
  5. Low plasma NTproBNP.

Exclusion Criteria:

  1. Uncontrolled hypertension.
  2. More than moderate valvular disease.
  3. Estimated glomerular filtration rate <30mls/min.
  4. Atrial/supraventricular/ventricular arrhythmia requiring beta-blockade.
  5. Pregnancy.
  6. Unstable angina.
  7. Age <16 years

Sites / Locations

  • Royal Brompton and Harefield NHS Trust

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Withdrawal of therapy

Control

Arm Description

Gradual, supervised withdrawal of medical therapy over 4-16 weeks

Continuation of usually prescribed pharmacological therapy

Outcomes

Primary Outcome Measures

Heart failure relapse
Defined by one of the following: 1) A reduction in left ventricular ejection fraction; 2) An increase in left ventricular size; 3) An increase in serum biomarker concentration from baseline; 4) Clinical evidence of heart failure

Secondary Outcome Measures

Cardiopulmonary exercise testing with peak oxygen consumption
Change in peak oxygen consumption between baseline and follow-up test
Quality of life
Patient questionnaires - Kansas City Cardiomyopathy Questionnaire and Heart Failure Symptom Questionnaire (symptom scores are calculated on the basis of the participants' answers to the questionnaires)
Major adverse cardiovascular events (MACE) - safety end-point
MACE - unplanned cardiovascular (CV) hospitalisation, CV mortality and major adverse CV events (non-fatal myocardial infarction and non-fatal cerebrovascular accident)
Percentage of participants with new and sustained arrhythmias
New and sustained arrhythmias diagnosed during follow-up
Increase in left atrial volume as measured on cardiovascular magnetic resonance (CMR)
Increase in left atrial volume as measured on CMR (in millilitres)

Full Information

First Posted
April 14, 2016
Last Updated
November 8, 2017
Sponsor
Royal Brompton & Harefield NHS Foundation Trust
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1. Study Identification

Unique Protocol Identification Number
NCT02859311
Brief Title
A Pilot Feasibility Study in Recovered Heart Failure
Acronym
TRED
Official Title
A Pilot Feasibility Study in Recovered Heart Failure
Study Type
Interventional

2. Study Status

Record Verification Date
November 2017
Overall Recruitment Status
Unknown status
Study Start Date
April 2016 (undefined)
Primary Completion Date
August 2018 (Anticipated)
Study Completion Date
August 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Royal Brompton & Harefield NHS Foundation Trust

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
One third of patients diagnosed with heart failure demonstrate left ventricular reverse remodelling and recovery of cardiac function following a period of medical therapy. These patients have an excellent long-term prognosis. Whether they need to remain on long-term medical therapy is not clear. The investigators will investigate the safety of therapy withdrawal in patients with a previous diagnosis of heart failure and recovered cardiac function, in a randomised controlled trial.
Detailed Description
Patients with a previous diagnosis of heart failure, who have recovered cardiac function, without symptoms, normal serum biomarker concentrations and who are currently still taking heart failure medications, will be recruited. Participants will be randomised to withdrawal of therapy and control arms and will undergo imaging investigations and cardiopulmonary exercise tests at baseline along with serum biomarker tests. Those participants randomised to withdrawal of therapy will have a gradual, supervised reduction of medications. If, at anytime, there are signs of recurring heart failure, medications will be restarted. Participants in the control arm will continue their medical therapy as usual. Participants will be followed up with further biomarker testing, cardiopulmonary exercise testing and imaging investigations at 6 months. The primary end-point will be a relapse in heart failure, defined by adverse remodelling, increase in left ventricular size, rise in serum biomarkers or clinical evidence of heart failure as judged by the clinical team.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure
Keywords
Recovery

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Withdrawal of therapy
Arm Type
Experimental
Arm Description
Gradual, supervised withdrawal of medical therapy over 4-16 weeks
Arm Title
Control
Arm Type
No Intervention
Arm Description
Continuation of usually prescribed pharmacological therapy
Intervention Type
Drug
Intervention Name(s)
Withdrawal of therapy
Intervention Description
Withdrawal of heart failure therapies (angiotensin converting enzyme inhibitors, angiotensin receptor blockers, beta-blockers, mineralocorticoid receptor antagonists and loop diuretics)
Primary Outcome Measure Information:
Title
Heart failure relapse
Description
Defined by one of the following: 1) A reduction in left ventricular ejection fraction; 2) An increase in left ventricular size; 3) An increase in serum biomarker concentration from baseline; 4) Clinical evidence of heart failure
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Cardiopulmonary exercise testing with peak oxygen consumption
Description
Change in peak oxygen consumption between baseline and follow-up test
Time Frame
6 months
Title
Quality of life
Description
Patient questionnaires - Kansas City Cardiomyopathy Questionnaire and Heart Failure Symptom Questionnaire (symptom scores are calculated on the basis of the participants' answers to the questionnaires)
Time Frame
6 months
Title
Major adverse cardiovascular events (MACE) - safety end-point
Description
MACE - unplanned cardiovascular (CV) hospitalisation, CV mortality and major adverse CV events (non-fatal myocardial infarction and non-fatal cerebrovascular accident)
Time Frame
6 months
Title
Percentage of participants with new and sustained arrhythmias
Description
New and sustained arrhythmias diagnosed during follow-up
Time Frame
6 months
Title
Increase in left atrial volume as measured on cardiovascular magnetic resonance (CMR)
Description
Increase in left atrial volume as measured on CMR (in millilitres)
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Have an index diagnosis of heart failure confirmed by 2 independent operators based on clinical details. Be currently taking at least 1 of the following medications loop diuretic, betablocker, angiotension converting enzyme inhibitor/angiotensin receptor blocker and mineralocorticoid receptor antagonist. Have demonstrated evidence of left ventricular reverse remodelling following the initial diagnosis with subsequent improvement in ejection fraction to >50% and normalisation of left ventricular (LV) volumes. Have no symptoms of heart failure (NYHA Class 1). Low plasma NTproBNP. Exclusion Criteria: Uncontrolled hypertension. More than moderate valvular disease. Estimated glomerular filtration rate <30mls/min. Atrial/supraventricular/ventricular arrhythmia requiring beta-blockade. Pregnancy. Unstable angina. Age <16 years
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sanjay Prasad, MD
Organizational Affiliation
Royal Brompton and Harefield NHS Foundation Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
Royal Brompton and Harefield NHS Trust
City
London
ZIP/Postal Code
SW3 6NP
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
34119469
Citation
Halliday BP, Vazir A, Owen R, Gregson J, Wassall R, Lota AS, Khalique Z, Tayal U, Jones RE, Hammersley D, Pantazis A, Baksi AJ, Rosen S, Pennell DJ, Cowie MR, Cleland JGF, Prasad SK. Heart Rate as a Marker of Relapse During Withdrawal of Therapy in Recovered Dilated Cardiomyopathy. JACC Heart Fail. 2021 Jul;9(7):509-517. doi: 10.1016/j.jchf.2021.03.010. Epub 2021 Jun 9.
Results Reference
derived
PubMed Identifier
30429050
Citation
Halliday BP, Wassall R, Lota AS, Khalique Z, Gregson J, Newsome S, Jackson R, Rahneva T, Wage R, Smith G, Venneri L, Tayal U, Auger D, Midwinter W, Whiffin N, Rajani R, Dungu JN, Pantazis A, Cook SA, Ware JS, Baksi AJ, Pennell DJ, Rosen SD, Cowie MR, Cleland JGF, Prasad SK. Withdrawal of pharmacological treatment for heart failure in patients with recovered dilated cardiomyopathy (TRED-HF): an open-label, pilot, randomised trial. Lancet. 2019 Jan 5;393(10166):61-73. doi: 10.1016/S0140-6736(18)32484-X. Epub 2018 Nov 11.
Results Reference
derived

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A Pilot Feasibility Study in Recovered Heart Failure

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