Right Ventricular Apical Versus True Mid-septal Pacing (MS-R)

June 9, 2021 updated by: Pavel Osmancik, Charles University, Czech Republic

A Comparison Between Right Ventricular Apical Pacing and True Mid-septal Pacing, Verified With Computed Tomography: a Randomized Study

Background Right ventricular (RV) artificial apical pacing can negatively impact synchrony of left ventricular contraction. The pacing from the septum of the RV can present an advantage in terms of less expressed dyssynchrony and reduced negative impact on left ventricular (LV) function. However, results of randomized studies comparing apical and septal pacing are not uniform. All these results have been affected by improper implantation of the septal lead, with many apparently septal leads being, in fact, implanted off-septum. The aim of the study is to compare true septal pacing with other RV pacing locations.

Methods/Design This is a prospective, randomized, single center study. Patients with standard indications for cardiac pacing with the expectation of high percentage RV pacing will be enrolled. They will be randomized into apical and septal pacing. The real location of leads in patients randomized to septal pacing will be confirmed using cardiac CT. After cardiac CT, three groups of patients will be created: 1) apical pacing, 2) true septal (in which the position of the lead has been verified to be in the septum), and 3) apparent septal (in which the position of the lead was found to be off-septum). Primary end-point are changes in standard echocardiographic parameters (LV ejection fraction, LV end-systolic volume, and LV end-diastolic volume) and the concentration of N-terminal pro brain natriuretic peptide (NT-proBNP) from baseline to 6 months, 1 year and three years. Secondary end-points are changes in echo-parameters of LV synchrony.

Discussion It is hypothesized that correct septal pacing will be associated with reduce negative impact on the function of the left ventricle (i.e. smaller decreases in LV EF and smaller increases in LVEDV, LVESV) and NT-proBNP, and less expressed LV dyssynchrony.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

METHODS/DESIGN The study is planned as prospective, multicenter, randomized study. The study was approved by the local ethics committee, and written informed consent will be obtained before enrollment of patients.

Inclusion criteria will be the following:

  1. Indication for cardiac pacing based on recent guidelines of European Society of Cardiology (5)
  2. High degree atrio-ventricular (AV) block (AV block 2/1 or second degree AV block with resulting heart rate below 50), or atrial fibrillation with slow conduction to ventricles.
  3. A high probability of needing significant ventricular stimulation (more than 50%)
  4. Written informed consent.

Exclusion criteria will be the following:

  1. The absence of written informed consent
  2. Renal insufficiency (creatinine level more than 130 µmol/l)
  3. History of Iodine allergy
  4. Claustrophobia
  5. Significant valve disease (i.e. mitral insufficiency 75% and worse, moderate or severe aortic stenosis)
  6. Recent (within three months) acute coronary syndrome
  7. Planned cardiac surgery (coronary artery bypass grafting, valve surgery)
  8. Ejection fraction of left ventricle less than 50%
  9. Expected life expectancy less than 3 years
  10. Expected non-compliance.

End-points: there are three unique primary end-points: 1) changes in left ventricular end-systolic volume (LVESV) over time (from baseline to 6 months and 3 years), 2) changes in the left ventricular ejection fraction (LV EF) over time (from baseline to 6 months and 3 years) and 3) changes in concentration of N-terminal pro brain natriuretic peptide (NT-proBNP), from baseline to 6 months up to three years).

Secondary endpoints are changes in echocardiography parameters of left ventricular synchrony, changes in left ventricular end-diastolic volume (LVEDV) over time and changes in the quality of life, as assessed by the Minnesota Living with Heart Failure questionnaire, over time (from baseline to 6 months and 3 years).

Power calculation and statistical analysis: The sample size calculation was based on the following assumptions: the power of the test = 0.8 and a statistical significance border = 0.05. Based on information from previous trials regarding the effect of pacing on left ventricular volumes and parameters, it is assumed that there will be at least a 10% difference in the change of LV end-systolic volume (LVESV, measured from baseline to 3 years follow-up) between the group paced from apex and the group with true septal pacing. Based on previous results regarding the efficacy of true septal pacing, based on recent fluoroscopy criteria, it is assumed that approximately 40% of those randomized to the septal group will not have the lead located in the septum, but in the anterior wall. This means that 70 patients are needed in the apical group, 70 in the septal group and 70 in the apparent septal group to achieve statistical significance. Data analysis will be performed using standard tests (chi-square, Student t-test, Kruskal-Wallis test etc.) For data description, standard descriptive statistical methods will be used: absolute and relative frequencies for categorical data and the median with 5-95% percentiles for continuous data. For categorical variables, statistical analysis will be done using the χ2 or the Fisher exact test; for continuous variables, the Student t-test, Mann-Whitney U test or Kruskal-Wallis test will be used. Kaplan-Meier curves will be calculated for visualizing the occurrence of end-points during follow-up. The influence of patient characteristics on the occurrence of end-points will be calculated using logistic regression and the Cox proportional risk model, when appropriate.

Data analysis In the primary analysis, three groups of patients will be analyzed: 1) patients randomized to RV apical pacing (apex group); 2) patients with true septal pacing (true septal group, i.e. those randomized to septal pacing, in whom the location of the lead was confirmed (using cardiac CT) to actually be in the septum), and 3) patients with apparent septal pacing (apparent septal group, i.e. those randomized to septal pacing, in whom the lead location will be found to off-septum, based on cardiac CT). The primary goal of the study will be to confirm that true septal pacing is associated with fewer prominent negative effects on the left ventricle. A secondary goal is to determine if off-septum placement (i.e., apparent septal group) has similar negative consequences for the left ventricle as those seen in apical pacing. In a secondary analysis, the two original groups will be compared (i.e., the groups randomized to apical vs. septal pacing).

Echocardiographic evaluation All patients will undergo echocardiography before implantation and during follow-up. Echocardiography will be done in the left lateral decubitus position. Imaging will be performed using a commercially available echocardiographic system (VIVID 7, General Electric Ultrasound, Milwaukee, USA). Images will be obtained using a 3.5 Mega Hertz transducer, at a depth of 16 cm in the parasternal (long and short axis) and apical (two- and four-chamber images) views. Standard 2D and colour Doppler data, triggered by the Q R S complex, will be saved in cine-loop format. A minimum of three consecutive beats will be recorded from each view and the images will be digitally stored for off-line analysis (EchoPac 7.0.0, General Electric Ultrasound, Milwaukee, USA). Left ventricular end-systolic volume (LVESV), LV end-diastolic volume (LVEDV), and LV EF will be measured from the apical two- and four-chamber images, using the (modified biplane) Simpson's rule. (10) Parameters of interventricular and left ventricular dyssynchrony will be measured off-line using tissue Doppler.

Conventional tissue Doppler-based dyssynchrony indices will be determined; (11) the standard deviation (SD) in time to peak velocity in 12 mid and basal segments (Ts SD12), the difference in time to peak velocity between anteroseptal and posterior wall (Ts AsP), the difference in time to peak velocity between the septal and lateral wall (Ts SL) as well as the maximal difference in time to peak velocity in 6 basal segments (Ts Diff6). Moreover, newer recently published parameters of dyssynchrony, such as apical rocking or septal flash, will also be measured. (12)

Further examinations before implantation Patients will be asked to complete the Minnesota Living with Heart Failure Questionnaire and the concentration of NT-proBNP, in peripheral blood will be measured. Afterwards patients will be randomized to RV apical or RV septal pacing. Because it can be anticipated that not all leads intended for RV septal implantation will actually end up implanted in the RV septum (some will be in the free anterior wall or in the anteroseptal groove), the ratio of randomization will be 2/1 (mid-septal vs. apical).

Implantation will be done using the standard approach, i.e., using the subclavian or cephalic approach. Only active fixation leads will be used. The position of the lead in the RV apical group will be assessed by displaying the lead in the anteroposterior (AP), right anterior oblique (RAO) 30 and left anterior oblique (LAO) 40 projection and stored. For the septal pacing group, a 3D stylet with two angulations will be prepared, as proposed recently. (9) Initially, the distal end of a standard stylet will be manually shaped into a smooth large curve, in a single plane, over a length of about 20 cm using the barrel of a syringe. The lead, with this J-shape stylet, will be advanced into the RV and further to the pulmonary artery. Then the stylet will be withdrawn and an additional 90° curve angulation will be created with the distal 3 cm end of the stylet. The 3D stylet will be inserted into the lead, and by slight counterclockwise torque applied, the lead will be withdrawn from the pulmonary artery to the right ventricle. A "jump" is usually seen as the lead falls below the RV outflow tract. At that point, the lead is quickly advanced and forced against the mid-septum. This manipulation will be done using RAO 30, and the target position is in the middle of the cardiac contour. Before final lead fixation, the position of the lead will be checked in the LAO 40 (the lead should point toward the spine with an angle to the horizontal plane between 0 to 60°). Perioperative fluoroscopy images will be stored, and standard implant parameters will be measured (impedance, R wave amplitude, and threshold).

Cardiac CT will be performed 6-12 weeks after implantation to assess the true position of the RV lead in the heart. Before cardiac CT, lead dislodgement will be excluded by measuring standard lead parameters.

Image acquisition CT will be performed using a 256-detector-row CT scanner (Brilliance CT 256; Philips, Best, The Netherlands) with a tube voltage of 100 kilo Volt (kV), collimation of 2x128×0.625 mm, a pitch of 0.18, a rotation time of 0.27 s, and a slice thickness of 0.9 mm. A tri-phasic injection of 60 mL of contrast media (Ultravist 370, Bayer Healthcare Pharmaceuticals, New Jersey, USA) will be used. Initially, 50 mL of contrast agent will be administered at a flow rate of 4.0 mL/s, followed by 20 mL of 50% contrast/saline. Subsequently, a saline flush of 30 mL will be administered at a flow rate of 3.0 mL/s. Bolus tracking will be used for synchronization of the contrast medium injection during scanning. The region of interest will be the descending aorta. After enhancement reaches 140 hounsfield Units (HU), there will be 3-s post-threshold delay before the scan is commenced. Prospective ECG triggered dose modulation (mode "step and shoot") will be used, scanning 70-80% of the R - R interval. After examination, the displayed dose-length product (DLP) will be recorded to evaluate radiation dose.

Image post-processing Datasets will be transferred to an external workstation (Comprehensive Cardiac Analyses, Brilliance Workspace v 4.0, Philips Healthcare, Cleveland, USA) for off-line analysis. Axial slices, oblique reconstructions and maximum-intensity projection (MIP) images will be used for precise localization of the RV lead. According to the location of RV lead, septal group patients will be divided in two sub-groups: true septum group (i.e. patients randomize to septal pacing, in whom the lead is actually found to be in the septum) and apparent septum group (i.e. those randomized to the septal pacing, in whom the lead is found to be off-septum, and typically in the free anterior wall or in the anteroseptal groove). Because the apical position is easily visible with fluoroscopy, cardiac CT will be done only in the patients randomized to septal pacing.

Post-implantation follow-up and out-patient controls will be done at 6 months, 1 year, and 3 years. During each control, standard pacemaker parameters (impedance, threshold, and amplitude) will be measured, and the percentage of ventricular stimulation will be assessed. During each control, echocardiography will be done, NT-proBNP measured, and patients will be asked to fulfill the Minnesota questionnaire.

Study Type

Interventional

Enrollment (Anticipated)

200

Phase

  • Phase 4

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

  • Czechia
      • Prague, Czechia
        • Recruiting
        • Charles University in Prague

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

Indication for cardiac pacing.

Exclusion Criteria:

  • renal insufficiency
  • iod allergy
  • claustrophobia
  • significant valvular disease
  • recent acute coronary syndrome
  • planned cardiac surgery
  • ejection fraction of left ventricle less than 50%
  • live expectancy less than 3 years
  • expected non-compliance of the patient

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Pacing site - right ventricular apex
The intervention will be the implantation of the lead into the right ventricular apex
Procedure: Pacing site - the implantation in the right ventricular (RV) apex
Pacing site - RV apex. The lead will be implanted in the RV apex.
Other Names:
  • Pacing site - RV apex
Experimental: Pacing site - septum
The intervention will be the implantation of the lead into the septum.
Procedure: Pacing site - the implantation in the septum
Pacing site - septum. The lead will be implanted in the septum.
Other Names:
  • Pacing site - MS

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline in the left ventricular ejection fraction at 6 months
Time Frame: from baseline to 6 months
The changes over time in the left ventricular ejection fraction will be determined.
from baseline to 6 months
Change from baseline in the left ventricular end-systolic volume at 6 months
Time Frame: from baseline to 6 months
The changes over time in the left ventricular end-systolic volume will be determined.
from baseline to 6 months
Change from baseline in the concentration of N-terminal pro-Brain Natriuretic Peptide at 6 months
Time Frame: from baseline to 6 months
The changes over time in the concentration of the N-terminal pro-brain natriuretic peptide will be determined.
from baseline to 6 months
Change from baseline in the left ventricular ejection fraction at 3 years
Time Frame: from baseline to 3 years
The changes over time in the left ventricular ejection fraction will be determined.
from baseline to 3 years
Change from baseline in the left ventricular end-systolic volume at 3 years.
Time Frame: from baseline to 3 years
The changes over time in the left ventricular ejection fraction will be determined.
from baseline to 3 years
Change from baseline in the concentration of N-terminal pro-Brain Natriuretic Peptide at 3 years.
Time Frame: from baseline to 3 years
The changes over time in the concentration of the N-terminal pro-brain natriuretic peptide will be determined.
from baseline to 3 years

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline in dyssynchrony at 6 months
Time Frame: from baseline to 6 months
Echo parameters of dyssynchrony wil be measured.
from baseline to 6 months
Change from baseline in the left ventricular end-diastolic volume at 6 months
Time Frame: from baseline to 6 months
The changes over time in the left ventricular end-diastolic volume will be determined.
from baseline to 6 months
Change from baseline in dyssynchrony at 3 years.
Time Frame: from baseline to 3 years
Echo parameters of dyssynchrony wil be measured.
from baseline to 3 years
Change from baseline in the left ventricular end-diastolic volume at 3 years.
Time Frame: from baseline to 3 years
The changes over time in the left ventricular end-diastolic volume will be determined.
from baseline to 3 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Charles University, Czech Republic

Investigators

  • Principal Investigator: Pavel Osmancik, MD, PhD, 3rd Faculty of Medicine, Charles University Prague

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 1, 2014

Primary Completion (Anticipated)

December 1, 2022

Study Completion (Anticipated)

December 1, 2022

Study Registration Dates

First Submitted

March 24, 2015

First Submitted That Met QC Criteria

April 8, 2015

First Posted (Estimate)

April 9, 2015

Study Record Updates

Last Update Posted (Actual)

June 11, 2021

Last Update Submitted That Met QC Criteria

June 9, 2021

Last Verified

June 1, 2021

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • CharlesUCR

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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