Trials / Completed
CompletedNCT00146861
LIFE Study - Limiting Chronotropic Incompetence for Pacemaker Recipients
Limiting Chronotropic Incompetence for Pacemaker Recipients
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 1,500 (planned)
- Sponsor
- Boston Scientific Corporation · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study will compare how two different sensors inside the pacemaker may affect patients' quality of life.
Detailed description
The LIFE Study will estimate the prevalence of CI among a general sample of pacemaker patients and compare changes in quality of life and physical activity between patients randomized to receive rate response driven by either blended sensor or accelerometer. Changes in chronotropic response between CI patients randomized to either blended sensor or accelerometer will be compared. A sub-study will evaluate changes in functional capacity between CI patients randomized to either blended sensor or accelerometer.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | sensor programming |
Timeline
- Start date
- 2003-07-01
- Primary completion
- 2006-01-01
- Completion
- 2006-01-01
- First posted
- 2005-09-07
- Last updated
- 2017-05-18
Source: ClinicalTrials.gov record NCT00146861. Inclusion in this directory is not an endorsement.