SAPIEN XT THV with the NovaFlex+ delivery system
DeviceEdwards SAPIEN XT™ Transcatheter Heart Valve along with NovaFlex+ delivery system
NCT Number: NCT03314857
To evaluate the safety and effectiveness of the SAPIEN XT (Edwards Lifesciences, Irvine, California) transcatheter heart valve implantation (TAVI) in Chinese patients with symptomatic severe calcific aortic stenosis who are considered at high risk for surgical valve replacement.
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Notify Me60 year and older
All sexes
Interventional
Not applicable
WestChina Hospital, Sichuan University, Sichuan, Chengdu, China
Edwards SAPIEN XT™ Transcatheter Heart Valve and NovaFlex+ delivery system will be used for this study.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Edwards SAPIEN XT™ Transcatheter Heart Valve along with NovaFlex+ delivery system
Time frame: 30 days
All of the deaths that occurred in this population regardless of the cause.
Time frame: 30 days
All of the deaths that occurred in this population due to a cardiovascular issue.
Time frame: 30 days
Total number of participates with a stroke.
Edwards Lifesciences
Industry
Safety and Effectiveness of Edwards Lifesciences SAPIEN XT Transcatheter Heart Valve in the Chinese Population
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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