Clinical Trials Directory

Trials / Completed

CompletedNCT00949715

Optimize RV Follow-up Selective Site Pacing Clinical Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
67 (actual)
Sponsor
Medtronic Cardiac Rhythm and Heart Failure · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of the Optimize RV Follow-Up study is to determine the long-term effect of selective site pacing. Selective site pacing refers to which area of the right ventricle the lead is placed. The goal of selective site pacing is to improve how the heart contracts when paced.

Detailed description

The Optimize RV Follow-Up Selective Site Pacing Clinical Trial is open to subjects that were previously enrolled in the Optimize RV Selective Site Pacing Clinical Trial.

Conditions

Interventions

TypeNameDescription
DEVICEMedtronic or Vitatron Dual-Chamber PacemakerA Medtronic or Vitatron market-approved dual-chamber implantable pulse generator (IPG) with atrial tachycardia/atrial fibrillation (AT/AF) trending ability
DEVICEMedtronic SelectSecure 3830 LeadMedtronic market-approved SelectSecure Model 3830 bipolar pacing lead

Timeline

Start date
2009-09-01
Primary completion
2011-04-01
Completion
2011-12-01
First posted
2009-07-30
Last updated
2018-02-15
Results posted
2013-10-01

Locations

12 sites across 3 countries: United States, Israel, Italy

Source: ClinicalTrials.gov record NCT00949715. Inclusion in this directory is not an endorsement.