Trials / Completed
CompletedNCT00291564
Ensure Cardiac Resynchronization Therapy Study
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 430 (planned)
- Sponsor
- Medtronic Cardiac Rhythm and Heart Failure · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to gather information on how doctors program particular settings on cardiac resynchronization therapy implantable cardiac defibrillators (CRT-Ds), to analyze how these settings affect the amount of cardiac resynchronization therapy (CRT) patients receive and to evaluate the therapy approach for converting abnormally fast heartbeats into normal heartbeats. There are no experimental devices or procedures involved in this study.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Cardiac Resynchronization Therapy Device |
Timeline
- Start date
- 2004-05-01
- Completion
- 2006-02-01
- First posted
- 2006-02-14
- Last updated
- 2007-12-21
Locations
32 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT00291564. Inclusion in this directory is not an endorsement.