RhytmiaPVC: The Rhytmia System to Determine the Precise Location and Potential Mechanism of Premature Contractions

Sponsor
University Hospital, Toulouse (Other)
Overall Status
Unknown status
CT.gov ID
NCT03460535
Collaborator
Boston Scientific Group (Other)
20
1
23.6
0.8

Study Details

Study Description

Brief Summary

This is a purely observational project and the objectives are to record and analyze the local potentials at the site of Premature Ventricular Contraction (VPC) focus through the Rhythmia system, ti determine the short and long-term success of the procedure and compare it to the existing literature about standard procedures, to highlight the advantages of the system compared to conventional mapping and to characterize optimal pace map or activation map as achieved by the Rhythmia system.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    This is a purely observational study. No special methodology choice, no comparison.

    The study want to find the determination of precise location of the focus and mechanisms involved constitutes a challenge for conventional electrophysiology, even with tridimensional systems, because of the time needed for accurate delineation of the location (due to the sometimes unfrequent Ventricular Premature Beats (VPB)) and to the insufficient mapping density or inadequate signal characteristics. The Rhythmia system could allow better determination of the focus location in relation to the anatomical structures, especially with unfrequent VPB, because of the available high density mapping due to the number of closed high-resolution electrodes located on the Orion catheter. Better delineation of the true focus origin and of the mechanisms involved (automaticity vs re-entry) may be of useful help for better understanding and efficient therapy.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    20 participants
    Observational Model:
    Case-Only
    Time Perspective:
    Prospective
    Official Title:
    Use of the Rhytmia System for Determining the Precise Location and Potential Mechanism of Premature Ventricular Contractions
    Actual Study Start Date :
    Jun 14, 2017
    Anticipated Primary Completion Date :
    Jun 1, 2019
    Anticipated Study Completion Date :
    Jun 1, 2019

    Outcome Measures

    Primary Outcome Measures

    1. Determining the surface of optimal pace map or activation map [One year]

      To evaluate the area of isochronal earliest activation of PVC (Premature Ventricular Contraction), based on unipolar or bipolar activation : correlations will be made with the suspected endocardial or epicardial/intra-mural location of the focus. This technic may reduce the area of perfect pace-mapping and possibly more accurately locate the focus.

    Secondary Outcome Measures

    1. Record the local potentials at the site of PVC focus through the Rhythmia system [One year]

      Pacing from any electrode being in close contact with the endocardial surface and comparing the paced QRS to the spontaneous VPC (automatic calculation available on Bard ElectroPhysiology (EP) system). Describe and analyze the local signals recorded from the Orion catheter at the site of the PVC focus. by looking for prepotentials as a surrogate of local abnormal automaticity, for local discrete scar and local late potentials favouring local reentry as a cause for PVC, determining the local activation characteristics of VPC (surface of local breakthrough, velocity and direction of activation.

    2. Determine the short success of the procedure [One year]

      Determine by repeated Holter recordings, and the relation to the findings made during the procedure (endocardial or suspected epicardial focus), mechanism

    3. Determine long-term success of the procedure and compare it to the existing [One year]

      Determine by repeated Holter recordings, and the relation to the findings made during the procedure (endocardial or suspected epicardial focus), mechanism

    4. Characterize optimal pace map or activation map as achieved by the Rhythmia system [One year]

      Evaluate the surface of perfect pace-mapping using the Orion catheter, by pacing from any electrode being in close contact with the endocardial surface and comparing the paced QRS to a template of the spontaneous VPC

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • patients with symptomatic monomorphic PVC with or without heart disease refractory to anti arrhythmic drugs

    • patients with dilated cardiomyopathy and altered Left Ventricular Ejection Fraction (LVEF) suspected to be causes by frequent monomorphic VPC

    • patients with malignant ventricular arrhythmias reproducibly induced by monomorphic PVC

    Exclusion Criteria:
    • patients with non-symptomatic VPC and without cardiomyopathy

    • patients under 18 yo

    • pregnant women

    • patients with polymorphic PVC arising from clearly different areas

    • patient protected by the french law: guardianship and Trusteeship

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University Hospital Toulouse Toulouse France 31059

    Sponsors and Collaborators

    • University Hospital, Toulouse
    • Boston Scientific Group

    Investigators

    • Principal Investigator: Philippe Maury, MD, University Hospital, Toulouse

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University Hospital, Toulouse
    ClinicalTrials.gov Identifier:
    NCT03460535
    Other Study ID Numbers:
    • RC31/16/8916
    • 2017-A00777-46
    First Posted:
    Mar 9, 2018
    Last Update Posted:
    Mar 9, 2018
    Last Verified:
    Mar 1, 2018
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by University Hospital, Toulouse
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 9, 2018