Clinical Trials Directory

Trials / Completed

CompletedNCT01015859

Spontaneous Atrioventricular Conduction Preservation

A Prospective Canadian Multi-center Randomized Study of the Benefits of Spontaneous Atrioventricular Conduction (Can Save R)

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
370 (actual)
Sponsor
Montreal Heart Institute · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The aims of this study are to assess the clinical benefits resulting from SafeR by comparison with standard dual chamber programming (DDD) with a long atrioventricular (AV) delay. The benefits will be assessed by comparing the percentage of ventricular pacing, the incidence of atrial arrhythmias, and the evolution of the hemodynamic status as observed through echo parameter and atrial natriuretic peptide/brain natriuretic peptide (ANP/BNP) measurements.

Conditions

Interventions

TypeNameDescription
DEVICEPacing modeTo determine which mode (DDD vs AAI SafeR)minimizes ventricular pacing

Timeline

Start date
2006-06-01
Primary completion
2012-08-01
Completion
2013-10-01
First posted
2009-11-18
Last updated
2013-10-30

Locations

9 sites across 1 country: Canada

Source: ClinicalTrials.gov record NCT01015859. Inclusion in this directory is not an endorsement.