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Pacing in Heart Failure With Preserved LVEF (MAPPLE)

Primary Purpose

Heart Failure

Status
Enrolling by invitation
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
CRT-pacemaker device set to Routine Medical Therapy
CRT-pacemaker device set to Routine Medical Therapy + LVP
CRT-pacemaker device set to Routine Medical Therapy + BiVP
Sponsored by
Cardiff and Vale University Health Board
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Heart Failure

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Clinical features consistent with heart failure. All patients will have symptoms of moderate to severe heart failure with New York Heart Association (NHYA) classification III or IV symptoms (for at least 3 months).
  2. LV Ejection Fraction less or equal to 50%, with no evidence of significant valvular disease, no hypertrophic or restrictive cardiomyopathy, and no evidence of pericardial constriction.
  3. A peak Vo2max less than 80% predicted, with respiratory exchange ratio (RER) more than 1 and a pattern of gas exchange on metabolic exercise testing indicating a cardiac cause for limitation.
  4. Additionally all patients will have demonstrated evidence of septal flattening during exercise using contrast echocardiography.

Exclusion Criteria:

  1. Inability to provide informed consent.
  2. Enrolment in other clinical studies.
  3. BMI more than 35
  4. Objective evidence of significant lung disease on formal lung function testing
  5. Previous (within three months) or scheduled coronary revascularisation or other cardiac surgery
  6. Acute coronary syndrome (within the previous three months)
  7. Renal insufficiency requiring haemodialysis
  8. Life expectancy less than 6 months
  9. Prosthetic heart valves
  10. Blood coagulation disorders
  11. Immunocompromised patients (e.g. AIDS, patients on steroids, cytotoxic drugs, and radiation therapy)

Sites / Locations

  • University Hospital Wales

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Sham Comparator

Experimental

Experimental

Arm Label

Routine Medical Therapy

Routine Medical Therapy + LVP

Routine Medical Therapy + BiVP

Arm Description

Routine Medical Therapy

Routine Medical Therapy + LVP

Routine Medical Therapy + BiVP

Outcomes

Primary Outcome Measures

Change in septal radius of curvature (corrected for LV area) between rest and peak exercise on stress echocardiography across the three pacing states.

Secondary Outcome Measures

Change in LV area between rest and exercise across the three pacing states
Change in Systolic and Diastolic mechanical Dyssynchrony Assessment on echocardiography across the three pacing states
Change in rest and exercise E/E' on echocardiography across the three pacing states

Full Information

First Posted
June 22, 2017
Last Updated
July 20, 2023
Sponsor
Cardiff and Vale University Health Board
Collaborators
Norfolk and Norwich University Hospitals NHS Foundation Trust, Cardiff Metropolitan University
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1. Study Identification

Unique Protocol Identification Number
NCT03215849
Brief Title
Pacing in Heart Failure With Preserved LVEF
Acronym
MAPPLE
Official Title
The Effect of Biventricular Pacing in Heart Failure With Preserved Left Ventricular Ejection Fraction: A Pilot Mechanistic Analysis
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Enrolling by invitation
Study Start Date
August 18, 2023 (Anticipated)
Primary Completion Date
March 31, 2024 (Anticipated)
Study Completion Date
March 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Cardiff and Vale University Health Board
Collaborators
Norfolk and Norwich University Hospitals NHS Foundation Trust, Cardiff Metropolitan University

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
A random-order cross-over pilot trial of a CE marked device (pacemaker) outside its current intended purposes. The study will comprise 10 patients. Recruitment of patients will take place from The University Hospital of Wales (Cardiff & Vale University Health Board [CVUHB]). All patients recruited will have septal flattening during exercise demonstrated using contrast stress (exercise) echocardiography. All 10 patients will be implanted with a CRT-pacemaker device and will be tested on all three of the following settings on separate visits (with a gap of up to 5 days between visits) in random order: Routine Medical Therapy Routine Medical Therapy + LVP Routine Medical Therapy + BiVP

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
10 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Routine Medical Therapy
Arm Type
Sham Comparator
Arm Description
Routine Medical Therapy
Arm Title
Routine Medical Therapy + LVP
Arm Type
Experimental
Arm Description
Routine Medical Therapy + LVP
Arm Title
Routine Medical Therapy + BiVP
Arm Type
Experimental
Arm Description
Routine Medical Therapy + BiVP
Intervention Type
Device
Intervention Name(s)
CRT-pacemaker device set to Routine Medical Therapy
Intervention Description
Medtronic Serena™ QUAD CRT-P MRI™ SureScan™ W4TR05 set to Routine Medical Therapy
Intervention Type
Device
Intervention Name(s)
CRT-pacemaker device set to Routine Medical Therapy + LVP
Intervention Description
Medtronic Serena™ QUAD CRT-P MRI™ SureScan™ W4TR05 set to Routine Medical Therapy + LVP
Intervention Type
Device
Intervention Name(s)
CRT-pacemaker device set to Routine Medical Therapy + BiVP
Intervention Description
Medtronic Serena™ QUAD CRT-P MRI™ SureScan™ W4TR05 set to Routine Medical Therapy + BiVP
Primary Outcome Measure Information:
Title
Change in septal radius of curvature (corrected for LV area) between rest and peak exercise on stress echocardiography across the three pacing states.
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Change in LV area between rest and exercise across the three pacing states
Time Frame
12 weeks
Title
Change in Systolic and Diastolic mechanical Dyssynchrony Assessment on echocardiography across the three pacing states
Time Frame
12 weeks
Title
Change in rest and exercise E/E' on echocardiography across the three pacing states
Time Frame
12 weeks

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Clinical features consistent with heart failure. All patients will have symptoms of moderate to severe heart failure with New York Heart Association (NHYA) classification III or IV symptoms (for at least 3 months). LV Ejection Fraction less or equal to 50%, with no evidence of significant valvular disease, no hypertrophic or restrictive cardiomyopathy, and no evidence of pericardial constriction. Additionally all patients will have demonstrated evidence of septal flattening during exercise using contrast echocardiography. Adults (over 18 years) Negative test for Covid during surgical pre-assessment, and adherence to prescribed self-isolation before implantation. Two weeks or more following final dose of vaccination against coronavirus. Exclusion Criteria: Inability to provide informed consent. Enrolment in other clinical studies. BMI more than 35 Objective evidence of significant lung disease on formal lung function testing Previous (within three months) or scheduled coronary revascularisation or other cardiac surgery Acute coronary syndrome (within the previous three months) History of atrial fibrillation (AF) Renal insufficiency requiring haemodialysis Life expectancy less than 6 months Prosthetic heart valves Blood coagulation disorders Immunocompromised patients (e.g. AIDS, patients on steroids, cytotoxic drugs, and radiation therapy) Currently pregnant, or intending to conceive. Recent positive Covid test (up to 14 days prior to pre-assessment).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Zaheer Yousef
Organizational Affiliation
Cardiff and Vale University Health Board
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital Wales
City
Cardiff
ZIP/Postal Code
CF14 4UJ
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Pacing in Heart Failure With Preserved LVEF

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