Natural Evolution of AV Conduction Disorders in Patients Implanted With Cardiac Pacemakers
Completed
- Conditions
- Patients Implanted With a Pacemaker
- Registration Number
- NCT00531037
- Lead Sponsor
- LivaNova
- Brief Summary
Observational study to assess AV block incidence and their evolution according to paroxysmal atrial arrhythmia.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 1440
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
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method High degree AV blocks 2 years
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (129)
Baptist Princeton Birmingham
🇺🇸Birmingham, Alabama, United States
Tennessee Valley Sheffield
🇺🇸Sheffield, Alabama, United States
Cardiovascular Assoc. Of Mesa
🇺🇸Mesa, Arizona, United States
O'Connor Hospital San Jose
🇺🇸San Jose, California, United States
Piedmont hospital
🇺🇸Piedmont, Georgia, United States
University of Mississippi Medical Center
🇺🇸Mississippi, Mississippi, United States
St. Francis Hospital Tulsa
🇺🇸Tulsa, Oklahoma, United States
Az St- Blasius
🇧🇪Dendermonde, Belgium
Ch de Huy
🇧🇪HUY, Belgium
Heilig Hart Ziekenhuis MOL
🇧🇪MOL, Belgium
Scroll for more (119 remaining)Baptist Princeton Birmingham🇺🇸Birmingham, Alabama, United States