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临床试验/NCT05721001
NCT05721001进行中(未招募)不适用

NEO - E-vita Open Neo Treatment of Aortic Arch Aneurysms and Dissections

JOTEC GmbH23 个研究点 分布在 1 个国家目标入组 130 人开始时间: 2023年1月11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
130
试验地点
23
主要终点
Mortality

研究概览

简要总结

Observational, prospective/retrospective, non-randomised, non-comparative, multicentre cohort study.

Primary objective is evaluation of in-hospital all-cause mortality after treatment of extensive acute and chronic aortic pathologies with E-vita OPEN NEO.

详细描述

Objectives

Primary objective:

• Evaluation of in-hospital all-cause mortality after treatment of extensive acute and chronic aortic pathologies with E-vita OPEN NEO

Secondary objective:

• Evaluation of the morbi-mortality in-hospital, 1 year and 3 years follow-up after treatment of extensive acute and chronic aortic pathologies with E-vita OPEN NEO.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Other

入排标准

性别
All
接受健康志愿者

入选标准

  • non-objection from the patient for data collection within this Registry
  • patient treated with E-vita Open NEO

排除标准

  • objection from the patient for data collection within this Registry

结局指标

主要结局

Mortality

时间窗: through study completion, an average of 3 years

Rate of in-hospital all-cause mortality

次要结局

  • Mortality(1 year and 3 years)
  • Neurological complications(At discharge, an average of 45 days, 1 year, 3 years)
  • Reinterventions(1 year, 3 years)
  • Severe Adverse Events(3 years)
  • Stroke(At discharge, an average of 45 days, 1 year, 3 years)
  • Paraplegia(At discharge, an average of 45 days, 1 year, 3 years)
  • Renal Insufficiency(At discharge, an average of 45 days, 1 year, 3 years)
  • Entry flow(At discharge, an average of 45 days, 1 year, 3 year)
  • Morbidity(1 year and 3 year)
  • Paraparesis(At discharge, an average of 45 days, 1 year, 3 years)
  • Permeability(1 year, 3 years)
  • Endoleaks(At discharge, an average of 45 days, 1 year, 3 years)
  • Malperfusion(At discharge, an average of 45 days, 1 year, 3 years)
  • Bleeding(At discharge, an average of 45 days, 1 year, 3 years)
  • False Lumen(At discharge, an average of 45 days, 1 year, 3 year)
  • Additional interventions(1 year, 3 year)

研究者

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

研究点 (23)

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French Registry Conducted on E-vita OPEN NEO | 临床试验