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Completed

NCT Number: NCT03314857

China XT: Safety and Effectiveness of Edwards Lifesciences SAPIEN XT THV in the Chinese Population

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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Key information

Age range

60 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

WestChina Hospital, Sichuan University, Sichuan, Chengdu, China

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About this study

Edwards SAPIEN XT™ Transcatheter Heart Valve and NovaFlex+ delivery system will be used for this study.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subjects who are considered to be operable and high risk for surgical valve replacement: 8 ≤ STS Score ≤ 15 or 15 ≤ Logistic EuroSCORE ≤ 40. If STS score is below 8 and/or Logistic EuroSCORE is below 15, patients should have other clinical or anatomical risk factors that would be considered high risk for surgery and documented by the heart team.
  • Severe symptomatic aortic stenosis requiring aortic valve replacement characterized by one or more of the following within 60 days prior to the index procedure: AVA < 0.8 cm2, Indexed AVA <0.5 cm2/m2, mean gradient > 40mmHg, or peak aortic jet velocity > 4.0m/sec.
  • NYHA Functional Class II or greater.
  • The study patient or the study patient's legal representative has been informed of the nature of the study, agrees to its provisions and has provided written informed consent as approved by the EC of the respective clinical site.
  • The study patient agrees to comply with all required post procedure follow-up visits.

Exclusion criteria

  • Evidence of an acute myocardial infarction ≤ 1 month (30 days) before the intended treatment.
  • Aortic valve is a congenital unicuspid or is non-calcified.
  • Aortic valve is bicuspid and the patient is less than 60 years old, or the aortic valve is bicuspid with no raphe (Sievers classification type 0).
  • Anomalous coronary artery that would interfere with proper placement of the valve.
  • Mixed aortic valve disease (aortic stenosis and aortic regurgitation with predominant aortic regurgitation >3+).

Treatment and study plan

SAPIEN XT THV with the NovaFlex+ delivery system

Device

Edwards SAPIEN XT™ Transcatheter Heart Valve along with NovaFlex+ delivery system

Primary outcomes

  1. All-cause Mortality

    Time frame: 30 days

    All of the deaths that occurred in this population regardless of the cause.

Secondary outcomes

  1. Cardiovascular Mortality

    Time frame: 30 days

    All of the deaths that occurred in this population due to a cardiovascular issue.

  2. Number of Participates With a Stroke

    Time frame: 30 days

    Total number of participates with a stroke.

Sponsors and collaborators

Lead sponsor

Edwards Lifesciences

Industry

Registry information

Official study title

Safety and Effectiveness of Edwards Lifesciences SAPIEN XT Transcatheter Heart Valve in the Chinese Population

Important dates

Study start
2017
Primary completion
2018
Study completion
2023
First posted
Oct 19, 2017
Registry last updated
Sep 5, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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