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ECG Belt to Assess Electrical Synchronization

Primary Purpose

Bradycardia, Heart Failure

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
ECG Belt
Sponsored by
Pugazhendhi Vijayaraman
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Bradycardia

Eligibility Criteria

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

Inclusion Criteria:

  1. Patients > 18 years of age
  2. Patient has a previously implanted LBBP lead for bradycardia indication or heart failure indication with one of the following at Geisinger within the last 5 years:

    • LBBP
    • LBBP+LV lead
    • HBP+LV
  3. Patient is willing to comply with all study procedures and be available for the duration of the study.

Exclusion Criteria:

  1. Inability to provide informed consent
  2. Pregnant
  3. Enrolled in a concurrent study that may confound the results of this study.

Sites / Locations

  • Geisinger Wyoming Valley

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

ECG Belt

Arm Description

ECG belt will be used to record ECG during baseline rhythm, LBBP in unipolar and bipolar configurations and / or during HOT-CRT using HBP or LBBP. These ECG belt characteristics would then be compared with baseline and existing data on RV pacing and traditional Biventricular pacing.

Outcomes

Primary Outcome Measures

• ECG Belt Analysis of Standard Deviation of Activation Times (SDAT) of LBBP Compared to Native Conduction
Change in SDAT following LBBP measured in ms using ECG Belt
• ECG Belt Analysis of Left Ventricular Activations Times (LVAT) of LBBP Compared to Baseline
Change in LV activation times measured in ms using ECG Belt
• ECG Belt Analysis of QRS Duration at Baseline Compared to Various LBBP Options
Change in QRS duration measured in ms using ECG Belt
• ECG Belt Analysis of LV Dispersion of HOT-CRT Compared to Baseline
LV dispersion measured using ECG Belt
• ECG Belt Analysis of RV Dispersion of HOT-CRT Compared to Baseline
RV dispersion measured using ECG Belt

Secondary Outcome Measures

Full Information

First Posted
September 29, 2020
Last Updated
July 28, 2022
Sponsor
Pugazhendhi Vijayaraman
Collaborators
Medtronic
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1. Study Identification

Unique Protocol Identification Number
NCT04583709
Brief Title
ECG Belt to Assess Electrical Synchronization
Official Title
ECG Belt to Assess Electrical Synchronization in Patients With Left Bundle Branch Pacing and His-Purkinje Conduction System Optimized Cardiac Resynchronization Therapy (ECG Belt)
Study Type
Interventional

2. Study Status

Record Verification Date
July 2022
Overall Recruitment Status
Completed
Study Start Date
January 13, 2021 (Actual)
Primary Completion Date
June 25, 2021 (Actual)
Study Completion Date
June 25, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Pugazhendhi Vijayaraman
Collaborators
Medtronic

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
No

5. Study Description

Brief Summary
The objective of the study is to assess the utility of ECG Belt to understand the conduction and ECG characteristics of Left Bundle Branch Pacing (LBBAP) and His-Optimized Cardiac Resynchronization Therapy (HOT-CRT) and compare with preexisting data in traditional Cardiac Resynchronization Therapy (CRT) and Right Ventricular Pacing (RVP).
Detailed Description
The objective of the study is to assess the utility of ECG Belt to understand the conduction and ECG characteristics of LBBP and HOT-CRT and compare with preexisting data in traditional CRT and RVP. Specific Objective: To demonstrate and establish electrical resynchronization using ECG Belt Research System in Left Bundle Branch Pacing (LBBP) and HOT-CRT. To assess ECG Belt derived native conduction parameters and compare them to LBBP and HOT-CRT. To compare with historic ECG belt parameters obtained for right ventricular pacing/ Biventricular pacing in prior studies. The ECG Belt study is a prospective, single-center, investigational, pre-market research study. The study team will identify all patients who satisfy the inclusion and exclusion criteria. The study team will evaluate the ECG Belt Research System to assess the electrical characteristics of conduction system pacing in patients with preexisting LBBP or HOT-CRT. Eligible patients would have successfully undergone LBBP using Medtronic 3830 lead. LBBP will be confirmed at implant using left bundle potentials recorded from the lead, ECG morphology during unipolar and bipolar pacing, peak LV activation time and lead depth in the LV septum by contrast at implant and 2D echo post-implant. ECG belt would be used to record ECG during baseline rhythm, LBBP in unipolar and bipolar configurations and / or during HOT-CRT using His-Bundle Pacing (HBP) or LBBP. These ECG belt characteristics would then be compared with baseline and existing data on Right Ventricular RV pacing and traditional Biventricular pacing.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
ECG Belt
Arm Type
Experimental
Arm Description
ECG belt will be used to record ECG during baseline rhythm, LBBP in unipolar and bipolar configurations and / or during HOT-CRT using HBP or LBBP. These ECG belt characteristics would then be compared with baseline and existing data on RV pacing and traditional Biventricular pacing.
Intervention Type
Device
Intervention Name(s)
ECG Belt
Intervention Description
ECG Belt Research System Procedure LBBP Native conduction RV pacing if available Bipolar LBBP Unipolar LBBP - nonselective and selective (different outputs) Fusion pacing with native conduction at different Atrioventricular (AV) delays HOT-CRT Native conduction HBP / LBBP HOT-CRT AV delay optimization. Medtronic Device (pacemaker/ICD) based Holter recording during the ECG belt recording
Primary Outcome Measure Information:
Title
• ECG Belt Analysis of Standard Deviation of Activation Times (SDAT) of LBBP Compared to Native Conduction
Description
Change in SDAT following LBBP measured in ms using ECG Belt
Time Frame
Visit 1 Baseline-50 minutes
Title
• ECG Belt Analysis of Left Ventricular Activations Times (LVAT) of LBBP Compared to Baseline
Description
Change in LV activation times measured in ms using ECG Belt
Time Frame
Visit 1 Baseline-50 minutes
Title
• ECG Belt Analysis of QRS Duration at Baseline Compared to Various LBBP Options
Description
Change in QRS duration measured in ms using ECG Belt
Time Frame
Visit 1 Baseline-50 minutes
Title
• ECG Belt Analysis of LV Dispersion of HOT-CRT Compared to Baseline
Description
LV dispersion measured using ECG Belt
Time Frame
Visit 1 Baseline- 50 minutes
Title
• ECG Belt Analysis of RV Dispersion of HOT-CRT Compared to Baseline
Description
RV dispersion measured using ECG Belt
Time Frame
Visit 1 Baseline- 50 minutes

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients > 18 years of age Patient has a previously implanted LBBP lead for bradycardia indication or heart failure indication with one of the following at Geisinger within the last 5 years: LBBP LBBP+LV lead HBP+LV Patient is willing to comply with all study procedures and be available for the duration of the study. Exclusion Criteria: Inability to provide informed consent Pregnant Enrolled in a concurrent study that may confound the results of this study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Pugazhendi Vijayaraman, MD
Organizational Affiliation
Geisinger Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Geisinger Wyoming Valley
City
Wilkes-Barre
State/Province
Pennsylvania
ZIP/Postal Code
18711
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
35907107
Citation
Vijayaraman P, Hughes G, Manganiello M, Johns A, Ghosh S. Non-invasive assessment of ventricular electrical heterogeneity to optimize left bundle branch area pacing. J Interv Card Electrophysiol. 2023 Aug;66(5):1103-1112. doi: 10.1007/s10840-022-01315-9. Epub 2022 Jul 30.
Results Reference
derived

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ECG Belt to Assess Electrical Synchronization

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