Clinical Trials Directory

Trials / Completed

CompletedNCT00814840

Efficiency Study of Triple-Site Cardiac Resynchronization in Patients With Heart Failure

Triple-Site Versus Standard Cardiac Resynchronization Therapy (TRUST CRT) Randomized Trial

Status
Completed
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
100 (actual)
Sponsor
Silesian Centre for Heart Diseases · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to assess the efficiency of permanent biventricular pacing using three ventricular leads in terms of reduction in adverse cardiac events rates, improvement in cardiac capacity and patients' functional status in subjects with congestive heart failure and a physiologic (sinus) rhythm.

Conditions

Interventions

TypeNameDescription
DEVICECardiac resynchronization pacemaker (InSync Sentry or Concerto, Medtronic, Minneapolis, MN,USA) with two intracardiac leadsCardiac resynchronization with two intraventricular leads: one in the right ventricle and one in the left ventricle (via the coronary sinus)
DEVICETriple-site cardiac resynchronizationCardiac resynchronization pacemaker (InSync Sentry or Concerto, Medtronic, Minneapolis, MN,USA) with three intraventricular leads: one in the right ventricle and two in the left ventricle (via the coronary sinus). Two left ventricular leads connected with Y-connector (Lead Adaptor 2827, Medtronic, Minneapolis, MN, USA)

Timeline

Start date
2008-02-01
Primary completion
2010-07-01
Completion
2015-01-01
First posted
2008-12-25
Last updated
2016-04-13

Locations

1 site across 1 country: Poland

Source: ClinicalTrials.gov record NCT00814840. Inclusion in this directory is not an endorsement.