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NCT00819793 · ClinicalTrials.gov registry record · NA
CentriMag Ventricular Assist System in Treating Failure-to-Wean From Cardiopulmonary Bypass
A NA study, sponsored by Abbott Medical Devices.
- Completed
- Registry status
- NA
- Development phase
- 32
- Enrollment target
NCT00819793: Completed NA study, sponsored by Abbott Medical Devices.
NCT00819793 is a NA study that has completed, run by Abbott Medical Devices. The registered enrollment target is 32 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00819793, a NA study, has completed, sponsored by Abbott Medical Devices.
- COMPLETED
- Registry status
- NA
- Development phase
- 32 participants
- Enrollment target
Study Summary
The purpose of the study is to evaluate the safety and effectiveness of the CentriMag ventricular assist system to help patients who have experienced heart failure during surgery and cannot be removed from cardiac bypass.
Primary Outcome
Number of patients alive 30 days after device implantation
Interventions
- DEVICE CentriMag Ventricular Assist System
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 32 participants |
| Start Date | 2008-10 |
| Est. Completion | 2013-09 |
| Phase | NA |
What the finished NCT00819793 record still lists
NCT00819793 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 32 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).
The record links to 0 conditions, and to 1 intervention - of which CentriMag Ventricular Assist System is the first listed.
NCT00819793 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00819793 about?
NCT00819793 is a clinical study titled "CentriMag Ventricular Assist System in Treating Failure-to-Wean From Cardiopulmonary Bypass". The purpose of the study is to evaluate the safety and effectiveness of the CentriMag ventricular assist system to help patients who have experienced heart failure during surgery and cannot be removed from cardiac bypass.
What is the current status of trial NCT00819793?
This trial is currently completed. It is a NA study. The enrollment target is 32 participants. The study started on 2008-10. Estimated completion is 2013-09.
What interventions are being tested in trial NCT00819793?
The interventions under investigation include: CentriMag Ventricular Assist System (DEVICE).
Who is sponsoring clinical trial NCT00819793?
This trial is sponsored by Abbott Medical Devices, which has 261 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00819793's enrollment target sits among peer trials
32 1578th of 2000 higher than 409 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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