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临床试验/NCT05082454
NCT05082454进行中(未招募)不适用

ASCEND - Post Market Clinical Follow-Up Study in Patients Treated with the On-X Ascending Aortic Prosthesis (AAP)

JOTEC GmbH11 个研究点 分布在 5 个国家目标入组 108 人开始时间: 2021年10月20日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
JOTEC GmbH
入组人数
108
试验地点
11
主要终点
Mortality

研究概览

简要总结

The ASCEND post-market clinical follow-up study is undertaken to evaluate safety and clinical performance of the On-X Ascending Aortic Prosthesis (AAP) used in surgical aortic valve replacement.

详细描述

In this study patients will be observed that receive an On-X AAP implant for the treatment of a diseased, damaged, or malfunctioning native or prosthetic heart valve. The On-X AAP will be implanted at the discretion of the treating physician. Participating physicians will be asked to provide their observations collected during routine care for patients he/she had decided to treat with the On-X AAP. Written informed consent, specifically allowing the use of clinical records for this observational study, will be obtained from every patient in Europe and every patient that is alive in the US prior to data collection where required. In Europe, every patient will be enrolled prospectively prior to the intervention.

In the US, patients can be enrolled retrospectively after the intervention or prospectively prior to the intervention. The data from patients who have died following their implant will be recorded in the database without the requirement for written informed consent after IRB approval.

The period of data collection will be approximately 60 + 6 months (depending on the date of the last follow-up visit) from the surgery for each patient.

Echocardiography images at prior to discharge, at 12 months, 60 months will be evaluated by a CoreLab. All adverse events defined in the Clinical Event Committee (CEC) charter will be adjudicated by the CEC.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Cross Sectional

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patient ≥ 18 years of age at time of On-X AAP implant
  • Patient understands and has signed the Informed Consent Form:
  • Prior to implant of On-X AAP or
  • Post implant (US only) or
  • Patient died prior to enrollment (US only)
  • Patient is willing and able to participate in follow-up

排除标准

  • Patient unable to tolerate anticoagulation therapy
  • Patient with active endocarditis at the time of his / her On-X AAP implant
  • Patient participates / participated in another clinical investigation which may interfere / may have interfered with the effectiveness of anticoagulation therapy
  • Patient has anomalous anatomy or medical, surgical, psychological or social history or conditions that, in the investigator's opinion, could limit the subject's ability to participate in the clinical investigation or to comply with follow-up requirements of the clinical investigation results
  • Patients in which On-X AAP is implanted in combination with AMDS or FET
  • Patient's life expectancy is less than 3 years in the opinion of the Investigator

结局指标

主要结局

Mortality

时间窗: at discharge to home or to rehabilitation

Rate of in-house all-cause mortality

次要结局

  • All-cause Mortality(30-day, 1 year, 2 years, 3 years, 4 years, 5 years)
  • Valve-related mortality(30-day, 1 year, 2 years, 3 years, 4 years, 5 years)
  • Reoperation(30-day, 1 year, 2 years, 3 years, 4 years, 5 years)
  • Explant(30-day, 1 year, 2 years, 3 years, 4 years, 5 years)
  • Endocarditis(30-day, 1 year, 2 years, 3 years, 4 years, 5 years)
  • Embolism(30-day, 1 year, 2 years, 3 years, 4 years, 5 years)
  • Thromboembolism(30-day, 1 year, 2 years, 3 years, 4 years, 5 years)
  • Bleeding(30-day, 1 year, 2 years, 3 years, 4 years, 5 years)
  • Transient ischemic attack(30-day, 1 year, 2 years, 3 years, 4 years, 5 years)
  • Stroke(30-day, 1 year, 2 years, 3 years, 4 years, 5 years)
  • Ischemic stroke(30-day, 1 year, 2 years, 3 years, 4 years, 5 years)
  • Hemorrhagic stroke(30-day, 1 year, 2 years, 3 years, 4 years, 5 years)
  • Valve deterioration(30-day, 1 year, 2 years, 3 years, 4 years, 5 years)
  • Non-structural dysfunction(30-day, 1 year, 2 years, 3 years, 4 years, 5 years)
  • Valve thrombosis(30-day, 1 year, 2 years, 3 years, 4 years, 5 years)
  • NYHA(1 year, 3 years, 5 years)

研究者

发起方
JOTEC GmbH
申办方类型
Industry
责任方
Sponsor

研究点 (11)

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