Tailor-CRT: Better Application of Cardiac Resynchronization Therapy
Primary Purpose
Heart Failure, Left Bundle-Branch Block
Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Cardiac Resynchronization Therapy
Sponsored by
About this trial
This is an interventional treatment trial for Heart Failure focused on measuring Cardiac Resynchronization Therapy, LV lead position, Device programming, Optimization, Vectorcardiography
Eligibility Criteria
Inclusion Criteria:
- Chronic heart failure with NYHA functional class II-IV
- Left ventricular ejection fraction (LVEF) < 35%
- Left bundle-branch block (LBBB) with QRS duration > 120 ms
- In sinus rhythm
Exclusion Criteria:
- Atrial fibrillation
- ≥4 premature ventricular complexes on standard 12-lead ECG
- Age <18 years or > 80 years
- Incapable of giving informed consent
- Moderate to severe aortic valve stenosis
Sites / Locations
- Maastricht University Medical Centre
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
CRT implantation
Arm Description
Patients who have a class I indication for cardiac resynchronization therapy according to current international guidelines
Outcomes
Primary Outcome Measures
Correlation between the increase in LV dP/dtmax and the D-VCG derived QRS area, obtained at different AV- and VV-intervals.
The optimal AV- and VV-interval produces the maximal increase in LV dP/dtmax. It is investigated whether the maximal increase in LV dP/dtmax also corresponds to the minimal QRS area derived from the D-VCG. The correlations will be expressed by the Pearson Correlation coefficient.
Correlation between the increase in LV dP/dtmax and the LVLED or VCG derived QRS area, obtained at different potential LV lead positions
The optimal LV lead position produces the maximal increase in LV dP/dtmax. It is investigated whether the maximal increase in LV dP/dtmax also corresponds to the longest LVLED or the minimal QRS area derived from the VCG. The correlations will be expressed by the Pearson Correlation coefficient.
Secondary Outcome Measures
Correlations between QRS vector area, -angle and -amplitude derived from VCG and from D-VCG.
The correlations will be expressed by the Pearson Correlation coefficient.
Full Information
NCT ID
NCT02326493
First Posted
November 27, 2014
Last Updated
February 22, 2017
Sponsor
Maastricht University Medical Center
Collaborators
University Medical Center Groningen, Medtronic
1. Study Identification
Unique Protocol Identification Number
NCT02326493
Brief Title
Tailor-CRT: Better Application of Cardiac Resynchronization Therapy
Official Title
Tailor-CRT: Better Application of Cardiac Resynchronization Therapy by Automated and Improved Selection of Location and Timing of Stimulation
Study Type
Interventional
2. Study Status
Record Verification Date
September 2016
Overall Recruitment Status
Completed
Study Start Date
November 2014 (undefined)
Primary Completion Date
November 2016 (Actual)
Study Completion Date
November 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Maastricht University Medical Center
Collaborators
University Medical Center Groningen, Medtronic
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Approximately one third of patients treated with cardiac resynchronization therapy (CRT) do not derive any clinical benefit. CRT response can be improved by tailoring LV lead placement and programming of atrio-ventricular (AV) and inter-ventricular (VV) stimulation intervals to the individual patient. However, the best strategy to optimize lead positioning and device programming still remains to be established. Earlier work in our research group suggests that the vector cardiogram (VCG) can be used to determine the optimal LV lead position and AV- and VV-intervals, and pilot studies showed the feasibility to derive a VCG-like signal (D-VCG) from the implanted pacing electrodes. Other studies have suggested that the best position for the LV electrode is the region of latest electrical activation. The region of latest electrical activation can be identified by measuring the electrical delay on the LV lead (LVLED) during implantation. The objective of this study is to investigate whether D-VCG can be used to determine the optimal AV- and VV-interval and whether VCG and LVLED can be used to determine the optimal LV lead position.
Detailed Description
Cardiac resynchronization therapy (CRT) is an established treatment for heart failure (HF) patients with severe left ventricular (LV) systolic impairment and delayed electrical impulse conduction through the ventricles, such as left bundle-branch block (LBBB). Since initial approval of the therapy over 10 years ago, there have been hundreds of thousands of implants worldwide. In The Netherlands, currently more than 2000 CRT devices are implanted each year. In a heart with LBBB, electrical activation of the lateral LV free wall is delayed, which leads to dyssynchronous and inefficient LV mechanical contraction and compromised LV pump function. The positive impact of CRT on LV pump function is attributed to paced pre-excitation of the delayed activated lateral LV wall. CRT is most commonly applied by pacing the right ventricle (RV) and LV lateral wall (almost) simultaneously. This corrects the abnormal LV electrical activation and resynchronizes LV mechanical contraction, which in turn results in improved LV pump function.
Despite the striking effectiveness of CRT, 30-50% of apparently suitable patients show little or no improvement. Previous studies have shown that the response to CRT can be improved by tailoring LV lead placement and programming of atrioventricular (AV) and inter-ventricular (VV) stimulation intervals to the individual patient. In clinical practice, echocardiographic techniques are the most widely employed for CRT optimization. However these techniques are subject to large measurement errors and inter- and intra-observer variability. A more accurate technique is invasive assessment of acute hemodynamic response to CRT, with the most widely used invasive hemodynamic parameter being the maximum rate of LV systolic pressure rise (LVdP/dtmax). However, the invasive and time-consuming nature of this approach limits its use in clinical practice. Thus, the best strategy to optimize lead positioning and device programming still remains to be established.
Earlier work in our research group suggests that the vectorcardiogram (VCG) can be used to determine the optimal LV lead position and AV- and VV-intervals, and pilot studies showed the feasibility to derive a VCG-like signal (D-VCG) from the implanted pacing electrodes. Other studies have suggested that the best position for the LV electrode is the region of latest electrical activation. The region of latest electrical activation can be identified by measuring the electrical delay on the LV lead (LVLED) during implantation. Validation of these techniques for tailoring LV lead positioning and AV- and VV- stimulation intervals to the individual patient, will provide non-invasive and easy methods to optimize CRT application and improve response rate.
The objective of this study is to investigate whether D-VCG can be used to determine the optimal AV- and VV-interval and whether VCG and LVLED can be used to determine the optimal LV lead position. Validation of these techniques for tailoring LV lead positioning and AV- and VV- stimulation intervals to the individual patient, will provide non-invasive and easy methods to optimize CRT application and improve response rate.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure, Left Bundle-Branch Block
Keywords
Cardiac Resynchronization Therapy, LV lead position, Device programming, Optimization, Vectorcardiography
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
28 (Actual)
8. Arms, Groups, and Interventions
Arm Title
CRT implantation
Arm Type
Experimental
Arm Description
Patients who have a class I indication for cardiac resynchronization therapy according to current international guidelines
Intervention Type
Device
Intervention Name(s)
Cardiac Resynchronization Therapy
Intervention Description
A CRT device will be implanted while performing extra hemodynamic (LV dP/dtmax) and electrical (LVLED, VCG, and D-VCG) measurements. Devices and leads from various vendors will be used.
Primary Outcome Measure Information:
Title
Correlation between the increase in LV dP/dtmax and the D-VCG derived QRS area, obtained at different AV- and VV-intervals.
Description
The optimal AV- and VV-interval produces the maximal increase in LV dP/dtmax. It is investigated whether the maximal increase in LV dP/dtmax also corresponds to the minimal QRS area derived from the D-VCG. The correlations will be expressed by the Pearson Correlation coefficient.
Time Frame
Acute measurements are performed for the duration of the CRT implantation procedure, an expected average of three hours
Title
Correlation between the increase in LV dP/dtmax and the LVLED or VCG derived QRS area, obtained at different potential LV lead positions
Description
The optimal LV lead position produces the maximal increase in LV dP/dtmax. It is investigated whether the maximal increase in LV dP/dtmax also corresponds to the longest LVLED or the minimal QRS area derived from the VCG. The correlations will be expressed by the Pearson Correlation coefficient.
Time Frame
Acute measurements are performed for the duration of the CRT implantation procedure, an expected average of three hours
Secondary Outcome Measure Information:
Title
Correlations between QRS vector area, -angle and -amplitude derived from VCG and from D-VCG.
Description
The correlations will be expressed by the Pearson Correlation coefficient.
Time Frame
Acute measurements are performed for the duration of the CRT implantation procedure, an expected average of three hours
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Chronic heart failure with NYHA functional class II-IV
Left ventricular ejection fraction (LVEF) < 35%
Left bundle-branch block (LBBB) with QRS duration > 120 ms
In sinus rhythm
Exclusion Criteria:
Atrial fibrillation
≥4 premature ventricular complexes on standard 12-lead ECG
Age <18 years or > 80 years
Incapable of giving informed consent
Moderate to severe aortic valve stenosis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kevin Vernooy, MD, PhD
Organizational Affiliation
Maastricht University Medical Centre
Official's Role
Principal Investigator
Facility Information:
Facility Name
Maastricht University Medical Centre
City
Maastricht
State/Province
Limburg
ZIP/Postal Code
6202 AZ
Country
Netherlands
12. IPD Sharing Statement
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Tailor-CRT: Better Application of Cardiac Resynchronization Therapy
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