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NCT00654199 · ClinicalTrials.gov registry record
Ventricular Asynchrony in Cardiac Surgery Patients
A clinical trial, sponsored by Weill Medical College of Cornell University.
- Completed
- Registry status
- 20
- Enrollment target
NCT00654199: Completed study, sponsored by Weill Medical College of Cornell University.
NCT00654199 is a clinical trial that has completed, run by Weill Medical College of Cornell University. The registered enrollment target is 20 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00654199 has completed, sponsored by Weill Medical College of Cornell University.
- COMPLETED
- Registry status
- 20 participants
- Enrollment target
Study Summary
The purpose of this study is to: 1. assess the existence of inter-ventricular and intra-ventricular asynchrony in cardiac surgery patients before (PRE) and after cardiopulmonary bypass surgery (POST) 2. investigate whether a modification of usual pacing practices (RA-LV pacing) can achieve inter- and intra-ventricular synchrony and improve heart function, as evaluated by hemodynamic and echocardiographic indexes, when compared with the patient's native rhythm (normal sinus rhythm (SR), or conventional pacing modes
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2006-05 |
| Est. Completion | 2009-10 |
What the finished NCT00654199 record still lists
NCT00654199 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 20 participants, a relatively small participant target.
The record links to 0 conditions, and to 0 interventions.
NCT00654199 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00654199 about?
NCT00654199 is a clinical study titled "Ventricular Asynchrony in Cardiac Surgery Patients". The purpose of this study is to: 1. assess the existence of inter-ventricular and intra-ventricular asynchrony in cardiac surgery patients before (PRE) and after cardiopulmonary bypass surgery (POST) 2. investigate whether a modification of usual pacing practices (RA-LV pacing) can achieve inter- a...
What is the current status of trial NCT00654199?
This trial is currently completed. The enrollment target is 20 participants. The study started on 2006-05. Estimated completion is 2009-10.
Who is sponsoring clinical trial NCT00654199?
This trial is sponsored by Weill Medical College of Cornell University, which has 701 total clinical trials registered on ClinicalTrials.gov.
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