Post-Market Surveillance Registry to Monitor Performance and Safety of V8 Device
Status: | Completed |
---|---|
Conditions: | Cardiology |
Therapuetic Areas: | Cardiology / Vascular Diseases |
Healthy: | No |
Age Range: | Any |
Updated: | 4/21/2016 |
Start Date: | March 2014 |
End Date: | December 2015 |
Transluminal Aortic Balloon Valvuloplasty Registry (TAB-R)
This registry is designed to monitor the real world clinical performance and safety of the
V8 device used to perform balloon aortic valvuloplasty (BAV). Additional analyses or
calculations may be obtained from the imaging or evaluations already performed per the
sites' standard of care
V8 device used to perform balloon aortic valvuloplasty (BAV). Additional analyses or
calculations may be obtained from the imaging or evaluations already performed per the
sites' standard of care
The study is an open-label observational study involving a minimum of 10 centers. A minimum
of 100 patients, including a minimum of 30 stand-alone balloon aortic valvuloplasty (BAV)
treatment patients, will be enrolled. Enrollment will continue until all 3 of these
conditions are met.
BAV-only patients will be followed through a 6-month post-treatment telephone follow up.
Patients treated with the V8 device for BAV as a bridge to transcatheter aortic valve
replacement (TAVR) or surgical aortic valve replacement (SAVR) or as an intraprocedural
predilatation prior to TAVR, will exit the study at the time of the TAVR or SAVR implant or
at 6 months post-BAV treatment, whichever comes first.
of 100 patients, including a minimum of 30 stand-alone balloon aortic valvuloplasty (BAV)
treatment patients, will be enrolled. Enrollment will continue until all 3 of these
conditions are met.
BAV-only patients will be followed through a 6-month post-treatment telephone follow up.
Patients treated with the V8 device for BAV as a bridge to transcatheter aortic valve
replacement (TAVR) or surgical aortic valve replacement (SAVR) or as an intraprocedural
predilatation prior to TAVR, will exit the study at the time of the TAVR or SAVR implant or
at 6 months post-BAV treatment, whichever comes first.
Inclusion Criteria:
- Symptomatic severe aortic stenosis (AS) patients who are not suitable candidates for
aortic valve replacement surgery at the time of BAV procedure.
- Subject meets the Indication For Use.
- Probable survival to hospital discharge.
- Subject is competent, willing to comply with evaluations, understands risks, benefits
and alternatives and has signed the Informed Consent Form. Alternatively, the legal
guardian of the patient is able to give consent to participate.
Exclusion Criteria:
- Patient has undergone previous AVR
- Greater or equal to 3+ aortic insufficiency by echocardiogram obtained prior to
planned BAV or intra-procedural predilation TAVR procedure
- Non-valvular AS
- Known congenital AV abnormality (e.g., bicuspid AV)
- Cardiogenic shock, as defined by a consistent systolic blood pressure <80 mmHg off
vasopressors or <90 mmHg on vasopressors.
- Bacterial endocarditis ≤ 12 months prior to planned BAV procedure
- Unable to take aspirin (acetyl salicylic acid, ASA) or thienopyridine
- Any illness or condition which, in the Investigator's judgment, will compromise
patient safety, or interfere with the interpretation of the treatment results
- Echocardiographic evidence of intracardiac mass, thrombus or vegetation.
We found this trial at
7
sites
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1211 Medical Center Dr
Nashville, Tennessee 37232
Nashville, Tennessee 37232
(615) 322-5000
Vanderbilt Univ Med Ctr Vanderbilt University Medical Center (VUMC) is a comprehensive healthcare facility dedicated...
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Univ of Washington Founded in 1861 by a private gift of 10 acres in what...
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Minneapolis, Minnesota 55407
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