Natural Evolution of AV Conduction Disorders in Patients Implanted With Cardiac Pacemakers

Overview

Observational study to assess AV block incidence and their evolution according to paroxysmal atrial arrhythmia.

Study Type

  • Study Type: Observational
  • Study Design
    • Time Perspective: Prospective
  • Study Primary Completion Date: December 2011

Clinical Trial Outcome Measures

Primary Measures

  • High degree AV blocks
    • Time Frame: 2 years

Participating in This Clinical Trial

Inclusion Criteria

  • Sinus Node Disease – Brady-Tachy Syndrome – Suspected or documented paroxysmal AVB Exclusion Criteria:

  • Permanent high degree AVB – Contra indication to the SafeR pacing mode – PR higher than 350 ms

Gender Eligibility: All

Minimum Age: 18 Years

Maximum Age: N/A

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • LivaNova
  • Provider of Information About this Clinical Study
    • Sponsor
  • Overall Official(s)
    • DEHARO Jean Claude, MD, Principal Investigator, CHU la Timone – Marseille

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