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The Effect of CRT on the Frank Starling Mechanism (CRT)

Primary Purpose

Pacemaker, Heartfailure

Status
Not yet recruiting
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Test Of The Frank Starling Mechanism - Adjustment Of Av Delay And Measurement Of Pre-load -Control
Other: Test Of The Frank Starling Mechanism - Adjustment Of Av Delay And Measurement Of Pre-load -CRT
Sponsored by
Guy's and St Thomas' NHS Foundation Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Pacemaker focused on measuring Frank Starling Mechanism, CRT

Eligibility Criteria

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

Inclusion Criteria: • Ability to provide informed consent to participate and willing to comply with the clinical investigation plan and follow-up schedule. Existing dual chamber pacemaker or ICD including atrial lead and RV lead. RV pacing percentage >40%. CRT group - Severe left ventricular systolic impairment (LVEF≤35%). Clinical symptoms of heart failure despite optimum medical therapy (NYHA class II-IV). Control group - LVEF >50%. Exclusion Criteria: • Previous treated with CRT (existing LV lead/His-Bundle lead/Left Bundle Branch Area lead). Persistent atrial fibrillation Female participants who are pregnant, lactating or planning pregnancy during the course of the study. Participation in other studies with active treatment / investigational arm

Sites / Locations

  • Guy's and St Thomas' NHS Trust

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

CRT Group

Control Group

Arm Description

CRT group: We will include patients with symptomatic heart failure (LV ejection fraction <35% on TTE, NYHA II-IV) and an RV pacing percentage of >40%, thus meeting ESC Criteria for CRT upgrade.

Control group: patients with an existing dual chamber pacemaker and with preserved ejection fraction

Outcomes

Primary Outcome Measures

Difference in starling mechanism
1. Difference in maximum change in stroke volume (SV) in millilitres with AV delay modification "Starling mechanics" pre-CRT versus post-CRT (difference between lowest and highest SV).

Secondary Outcome Measures

Left ventricular end-systolic volume (ml)
Difference in left ventricular end-systolic volume in millimetres recorded on echocardiogram
Left ventricular ejection fraction (%)
Difference in Left ventricular ejection fraction in percent measured on echocardiogram
Quality of life with heart failure symptoms
Quality of life in heart failure assessed by Minnesota Living with Heart Failure Questionnaire
Heart failure symptoms
New York Heart Association ( NYHA) class - breathlessness on different levels of exercise - from walking on the flat (NYHA 2) up to limited by breathlessness on little movement (NYHA 4)
Packer's clinical composite score
Difference in patient outcome measured by the clinical composite score - the score ranges from improved to unchanged or worsened
Difference in baseline Starling mechanics between CRT group and control group
Difference in stroke volume in millilitres during the pacing test (starling mechanism test) between the CRT and control group

Full Information

First Posted
July 31, 2023
Last Updated
August 8, 2023
Sponsor
Guy's and St Thomas' NHS Foundation Trust
Collaborators
King's College London
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1. Study Identification

Unique Protocol Identification Number
NCT05993585
Brief Title
The Effect of CRT on the Frank Starling Mechanism
Acronym
CRT
Official Title
The Effects of Cardiac Resynchronisation Therapy on the Frank Starling Mechanism in Patients With Heart Failure
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
August 4, 2023 (Anticipated)
Primary Completion Date
June 2, 2025 (Anticipated)
Study Completion Date
June 2, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Guy's and St Thomas' NHS Foundation Trust
Collaborators
King's College London

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
The investigators are examining a scientific principle called the Frank Starling Mechanism and how it relates to Cardiac Resynchronisation Therapy (CRT), a form of pacemaker therapy used in the treatment of heart failure. The Frank Starling Mechanism is an established biological principle. The law states that the stroke volume of the heart increases in response to an increase in the volume of blood in the ventricles, before contraction, when all other factors remain constant. In other words, the law states that the more blood enters the heart, the more blood is pumped out of the heart with any given beat. There is some evidence that in some patients with chronic heart conditions, the Frank Starling Mechanism is LESS EFFECTIVE, meaning that the heart is less able to cope with a reduction in heart pumping function over time. There is also evidence that treatment with CRT may IMPROVE the Frank Starling Mechanism - evidence for this has been shown in dog and mice hearts, however, has never been shown in humans. The investigators aim to conduct a study where subjects undergo an ultrasound scan of the heart (echocardiogram) whilst the participants pacemaker settings are temporarily changed. This allows the investigators to measure the pumping function of the heart as more blood enters the heart. The investigators will perform this test on 20 participants before and after CRT, as well as 20 participants who have pacemakers, but no heart failure. This study aims to test 3 hypotheses. In participants with pacemakers, a REDUCED Frank Starling Mechanism predicts which participants go on to develop heart failure. Treatment with CRT IMPROVES the Frank Starling Mechanism in participants with pacemakers and heart failure. The degree of improvement of the Frank Starling Mechanism after treatment with CRT predicts which participants will respond to this treatment.
Detailed Description
The primary research investigation in this study is a non-invasive test of the Frank Starling mechanism, which involves performing a transthoracic echocardiogram (ultrasound scan of the heart) whilst temporarily changing pacemaker settings to mimic conditions such as faster heart rates or increased blood flow to the heart. Measurements taken from the echocardiogram during these changes in pacemaker settings will be used to determine the effectiveness of the heart's Starling Mechanism. This test will last between 20-40 minutes. No special preparation is needed and participants will be able to go home immediately afterwards. Pacemaker settings will be returned to normal once the test is completed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pacemaker, Heartfailure
Keywords
Frank Starling Mechanism, CRT

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Single centre trial - observational cohort study
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
CRT Group
Arm Type
Experimental
Arm Description
CRT group: We will include patients with symptomatic heart failure (LV ejection fraction <35% on TTE, NYHA II-IV) and an RV pacing percentage of >40%, thus meeting ESC Criteria for CRT upgrade.
Arm Title
Control Group
Arm Type
Active Comparator
Arm Description
Control group: patients with an existing dual chamber pacemaker and with preserved ejection fraction
Intervention Type
Other
Intervention Name(s)
Test Of The Frank Starling Mechanism - Adjustment Of Av Delay And Measurement Of Pre-load -Control
Intervention Description
(Control Group): One test of the Starling mechanism Visit 1: Sign consent form, doctor assessment, electrocardiogram (ECG), Starling Test. If patients are in this category, this will be their only research visit
Intervention Type
Other
Intervention Name(s)
Other: Test Of The Frank Starling Mechanism - Adjustment Of Av Delay And Measurement Of Pre-load -CRT
Intervention Description
(CRT Group): Two tests of the Starling mechanisms Visit 1: Sign consent form, assessment by doctor, electrocardiogram (ECG), Test of the Starling mechanism Visit 2: CRT upgrade procedure - your Cardiologist will explain this procedure to you. Visit 3: CRT pacing check at 6 weeks post-procedure Visit 4: Assessment by doctor, ECG, Echocardiogram, Test of the Starling mechanism at 6 months post-procedure.
Primary Outcome Measure Information:
Title
Difference in starling mechanism
Description
1. Difference in maximum change in stroke volume (SV) in millilitres with AV delay modification "Starling mechanics" pre-CRT versus post-CRT (difference between lowest and highest SV).
Time Frame
Prior to pacing test (starling mechanism test) and after six months
Secondary Outcome Measure Information:
Title
Left ventricular end-systolic volume (ml)
Description
Difference in left ventricular end-systolic volume in millimetres recorded on echocardiogram
Time Frame
Prior to pacing test (starling mechanism test) and after six months
Title
Left ventricular ejection fraction (%)
Description
Difference in Left ventricular ejection fraction in percent measured on echocardiogram
Time Frame
Prior to pacing test (starling mechanism test) and after six months
Title
Quality of life with heart failure symptoms
Description
Quality of life in heart failure assessed by Minnesota Living with Heart Failure Questionnaire
Time Frame
Prior to pacing test (starling mechanism test) and after six months
Title
Heart failure symptoms
Description
New York Heart Association ( NYHA) class - breathlessness on different levels of exercise - from walking on the flat (NYHA 2) up to limited by breathlessness on little movement (NYHA 4)
Time Frame
Prior to pacing test (starling mechanism test) and after six months
Title
Packer's clinical composite score
Description
Difference in patient outcome measured by the clinical composite score - the score ranges from improved to unchanged or worsened
Time Frame
Prior to pacing test (starling mechanism test) and at six months
Title
Difference in baseline Starling mechanics between CRT group and control group
Description
Difference in stroke volume in millilitres during the pacing test (starling mechanism test) between the CRT and control group
Time Frame
Prior to pacing test (starling mechanism test) and at six months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: • Ability to provide informed consent to participate and willing to comply with the clinical investigation plan and follow-up schedule. Existing dual chamber pacemaker or ICD including atrial lead and RV lead. RV pacing percentage >40%. CRT group - Severe left ventricular systolic impairment (LVEF≤35%). Clinical symptoms of heart failure despite optimum medical therapy (NYHA class II-IV). Control group - LVEF >50%. Exclusion Criteria: • Previous treated with CRT (existing LV lead/His-Bundle lead/Left Bundle Branch Area lead). Persistent atrial fibrillation Female participants who are pregnant, lactating or planning pregnancy during the course of the study. Participation in other studies with active treatment / investigational arm
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sandra N Howell/Dr, Med State Exam, MSc, MSc
Phone
44 020 7188 9257
Email
sandra.howell@kcl.ac.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christopher Aldo Rinaldi/Professor, MD, FHRS
Organizational Affiliation
Guy's and St Thomas' NHS Trust
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Steven Niederer/Professor, PhD
Organizational Affiliation
King's College London
Official's Role
Principal Investigator
Facility Information:
Facility Name
Guy's and St Thomas' NHS Trust
City
London
ZIP/Postal Code
SE1 7EH
Country
United Kingdom
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sandra N Howell/Dr, Med State Exam, MSc, MSc
Phone
020 7188 9257
Email
sandra.howell@kcl.ac.uk
First Name & Middle Initial & Last Name & Degree
Christopher Aldo Rinaldi/Professor, MD, FHRS

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Non-identifiable data will be shared upon request
IPD Sharing Time Frame
Non-identifiable data will only be available after the end of the study
IPD Sharing Access Criteria
Fully anonymised data available upon request via email
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The Effect of CRT on the Frank Starling Mechanism

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