跳至主要内容
临床试验/NCT01636648
NCT01636648
终止
不适用

Enable I Long-term Follow-up Study

Medtronic Bakken Research Center6 个研究点 分布在 3 个国家目标入组 42 人2012年8月

概览

阶段
不适用
干预措施
未指定
疾病 / 适应症
Aortic Valve Stenosis
发起方
Medtronic Bakken Research Center
入组人数
42
试验地点
6
主要终点
Assess the Long-term safety of the Medtronic ATS Enable Aortic Bioprosthesis
状态
终止
最后更新
8年前

概览

简要总结

This was a prospective, non-randomized, multi-center, non-interventional post-market study. The study was a post-market long-term follow-up study based on the same cohort of patients (148 patients) enrolled in a previous investigational study from March 2007 to December 2009 (ATS 3f Enable™ Aortic Bioprosthesis Model 6000, number S2005) involving 10 European sites. Patient follow-up took place on a yearly basis up to 10 years after the implant/enrollment. The primary objective of this study was to evaluate the safety and effectiveness of the Medtronic ATS Enable Aortic Bioprosthesis during long-term follow-up.

As this was an observational study, safety and efficacy data were summarized and described. There was no statistically powered study hypothesis.

注册库
clinicaltrials.gov
开始日期
2012年8月
结束日期
2016年4月
最后更新
8年前
研究类型
Observational
性别
All

研究者

发起方
Medtronic Bakken Research Center
责任方
Sponsor

入排标准

入选标准

  • Patients who were enrolled and implanted for the ATS 3f Enable™ Aortic Bioprosthesis Model 6000, number S2005
  • Patient willing to sign the new Data Release form (DRF) or Patient Informed Consent (PIC) for the post-market study (what is applicable for the study due to local requirements and regulations)

排除标准

  • ATS 3f Enable™ Aortic Bioprosthesis Model 6000 was explanted
  • Patient died
  • Patient lost to follow-up
  • Patient withdrew consent

结局指标

主要结局

Assess the Long-term safety of the Medtronic ATS Enable Aortic Bioprosthesis

时间窗: 10 Years Post-Procedure

Long-term safety will be assessed by collecting following reported adverse events addressed: Migration, Valve Related Thromboembolism, Valvular thrombosis, Haemorrhage, Perivalvular Leak, Endocarditis, Hmolysis, Structural valve Deterioration, Non-Structural Dysfunction, Reoperation, Explant and Death.

Assess the Long-term Clinical Effectiveness of the Medtronic ATS Enable Aortic Bioprosthesis: NYHA Functional Classification

时间窗: 10 Years Post-Procedure

Long-term clinical effectiveness of the Aortic Bioprosthesis will be assessed by collecting the NYHA-class of enrolled subjects over a period of time, following surgery.

Long-term Effectiveness of the Medtronic ATS Enable Aortic Bioprosthesis: Hemodynamic Performance

时间窗: 10 Years Post-Procedure

Hemodynamic performance of the Aortic Bioprosthesis will be assessed by specific echocardiography measurements

研究点 (6)

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