Trials / Terminated
TerminatedNCT00944125
Dual Site Left Ventricular (LV) Pacing
Dual Site LV Pacing Study: Prospective Randomized Blinded Crossover Study of Patients Meeting Current CRT-D Indication to be Implanted With Dual LV Pacing Leads and Paced Chronically for at Least 6 Months Post-implant.
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 50 (actual)
- Sponsor
- Wake Forest University Health Sciences · Academic / Other
- Sex
- All
- Age
- 40 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to compare Dual LV (left ventricular) pacing to standard single LV pacing (BiV pacing) to see if Dual LV pacing: 1. Improves the way the heart's left ventricle functions 2. Decreases the number of hospital and clinic visits for heart failure related symptoms 3. Slows the rate patients experience certain heart failure symptoms 4. Reduces uncoordinated heart contractions
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Dual Site LV Pacing | Dual Site LV Pacing vs. BiV Pacing for a total of six months which includes two three crossover periods. |
| DEVICE | BiV Pacing | Dual Site LV Pacing vs. BiV Pacing for a total of six months which includes two three crossover periods. |
Timeline
- Start date
- 2009-06-01
- Primary completion
- 2013-07-01
- Completion
- 2013-07-01
- First posted
- 2009-07-23
- Last updated
- 2024-10-21
- Results posted
- 2016-03-21
Locations
2 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT00944125. Inclusion in this directory is not an endorsement.