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NCT00475709 · ClinicalTrials.gov registry record · NA
Aortic Valve Replacement With Trifecta(TM)
A NA study of Aortic Valve Stenosis and Aortic Valve Insufficiency, sponsored by Abbott Medical Devices.
- Completed
- Registry status
- NA
- Development phase
- 1,022
- Enrollment target
- 18
- Study locations
NCT00475709 is a NA study of Aortic Valve Stenosis and Aortic Valve Insufficiency that has completed, run by Abbott Medical Devices. The registered enrollment target is 1,022 participants, roughly in line with the 1,009-participant average among 30 other Aortic Valve Stenosis trials with a reported enrollment target. The trial reports 18 study locations across 13 states.
The verdict
NCT00475709, a NA study of Aortic Valve Stenosis and Aortic Valve Insufficiency, has completed, sponsored by Abbott Medical Devices.
- COMPLETED
- Registry status
- NA
- Development phase
- 1,022 participants
- Enrollment target
- 18
- Study locations
Study Summary
To confirm the clinical safety and effectiveness of the Trifecta valve.
Conditions Studied
Interventions
- DEVICE Trifecta Aortic Heart Valve
Study Locations (18)
Minnesota
- Abbott Northwestern Hospital - Minneapolis
- Mayo Clinic - Rochester
New York
- NYU Medical Center - New York
- Columbia University Medical Center - New York
North Carolina
- Mission Hospitals - Asheville
- Duke University Medical Center - Durham
Pennsylvania
- University of Pennsylvania Health System - Philadelphia
- Main Line Health Heart Center - Wynnewood
Texas
- Cardiothoracic and Vascular Surgeons - Austin
- Baylor College of Medicine - Houston
California
- USC Keck School of Medicine, Dept. of Cardiothoracic Surgery, USC University Hospital - Los Angeles
Florida
- Sarasota Memorial Hospital/Clinical Research Center - Sarasota
Illinois
- Loyola University Medical Center - Maywood
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,022 participants |
| Start Date | 2007-06 |
| Est. Completion | 2012-01 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00475709
The ClinicalTrials.gov registry entry for NCT00475709 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 1,022 participants, a figure that helps gauge the scale of data the investigators plan to collect, roughly in line with the 1,009-participant average among 30 other Aortic Valve Stenosis trials with a reported enrollment target. The listed sponsor is Abbott Medical Devices, which has 261 total studies on file at ClinicalTrials.gov.
The record links to 4 conditions, with Aortic Valve Stenosis appearing as the primary indexed condition, and to 1 intervention - of which Trifecta Aortic Heart Valve is the first listed.
NCT00475709 reports 18 study locations spanning 13 distinct geographic areas - top geographies include Minnesota, New York, North Carolina.
Frequently Asked Questions
What is clinical trial NCT00475709 about?
NCT00475709 is a clinical study titled "Aortic Valve Replacement With Trifecta(TM)". To confirm the clinical safety and effectiveness of the Trifecta valve.
What is the current status of trial NCT00475709?
This trial is currently completed. It is a NA study. The enrollment target is 1,022 participants. The study started on 2007-06. Estimated completion is 2012-01.
What conditions does trial NCT00475709 study?
This clinical trial studies the following conditions: Aortic Valve Stenosis, Aortic Valve Insufficiency, Regurgitation, Aortic Valve, Aortic Valve Incompetence.
What interventions are being tested in trial NCT00475709?
The interventions under investigation include: Trifecta Aortic Heart Valve (DEVICE).
Who is sponsoring clinical trial NCT00475709?
This trial is sponsored by Abbott Medical Devices, which has 261 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00475709 being conducted?
This trial has 18 study locations across California, Florida, Illinois, Michigan, Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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