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

Study Timeline

• Study Start: 2007-06
• Study First Submitted: 2007-09-17
• Study First Submitted QC: 2007-09-17
• Study First Posted: 2007-09-18
• Primary Completion: 2011-12
• Study Completion: 2011-12
• Status Verified: 2017-11
• Last Update Submitted: 2017-11-10
• Last Update Posted: 2017-11-14

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

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

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