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
| Type | Name | Description |
|---|---|---|
| DEVICE | Cardiac resynchronization pacemaker (InSync Sentry or Concerto, Medtronic, Minneapolis, MN,USA) with two intracardiac leads | Cardiac resynchronization with two intraventricular leads: one in the right ventricle and one in the left ventricle (via the coronary sinus) |
| DEVICE | Triple-site cardiac resynchronization | Cardiac 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.