跳至主要内容
临床试验/NCT05492383
NCT05492383已完成不适用

SAvvyWire™ EFficacy and SafEty in Transcatheter Aortic Valve Implantation Procedures (SAFE-TAVI)

Opsens, Inc.6 个研究点 分布在 1 个国家目标入组 119 人开始时间: 2022年10月25日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
Opsens, Inc.
入组人数
119
试验地点
6
主要终点
Percentage of patients with effective rapid pacing run

研究概览

简要总结

The purpose of the clinical investigation is to determine efficacy and safety of using the rapid pacing of SavvyWire™ during TAVI procedures.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

盲法说明

Investigation participant number only

入排标准

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

入选标准

  • •Subject is at least 18 years old
  • •Subject has a severe symptomatic AS undergoing a TAVI procedure
  • •Subject with a THV for which rapid pacing is considered necessary during valve implantation
  • •Subject agrees to participate in the study and is able to sign the informed consent form

排除标准

  • •Failure to provide signed informed consent
  • •Extremely horizontal aorta (aortic root angle ≥70°)
  • •Extreme tortuosity at the level of the iliofemoral arteries, thoracic or abdominal aorta
  • •Inability to receive full anticoagulation during the TAVI procedure
  • •Prohibitive surgical risk precluding (according to the Heart Team) conversion to open heart surgery in case of a life-threatening complication.

研究组 & 干预措施

Patients with severe symptomatic AS undergoing TAVI

Experimental

Patients with severe symptomatic AS undergoing a TAVI procedure with a THV for which rapid pacing is considered necessary during valve implantation

干预措施: TAVI (Device)

结局指标

主要结局

Percentage of patients with effective rapid pacing run

时间窗: during surgery

Effective rapid pacing will be defined as an adequate ventricular pacing capture by the SavvyWireTM leading to a reduction of systolic aortic pressure value \<60 mmHg.

次要结局

  • Percentage of patients with hemodynamic assessment without additional manipulation (pressure efficacy)(during surgery)
  • Percentage of patient with valve advancement to intended position (mechanical efficacy)(during surgery)
  • Presence of major complications (safety)(during surgery)

研究者

发起方
Opsens, Inc.
申办方类型
Industry
责任方
Sponsor

研究点 (6)

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