跳至主要内容
临床试验/NCT07664163
NCT07664163招募中不适用

SAIRO - Feasibility and Safety of the Tele-operated TAVIPILOT Robot Guided by TAVIPILOT Software During Transcatheter Aortic Valve Replacement (TAVR/TAVI)

Caranx Medical2 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2026年9月10日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
10
试验地点
2
主要终点
The investigational device-related safety will also be assessed by verifying the absence of major technical malfunctions

研究概览

简要总结

The TAVIPILOT robotic platform, developed by Caranx Medical is an advanced intraoperative robotic assistance system designed to enhance the precision of transcatheter aortic valve positioning during TAVR. The TAVIPILOT robotic platform includes the TAVIPILOT Software, Robot (when controlled by the user) and Loop (when guided by the Software). The system integrates with standard procedural workflows and enables remote manipulation of delivery system components, allowing for controlled, stable, and reproducible movements. TAVIPILOT devices facilitate accurate valve alignment and deployment, reducing operator variability. The robot is compatible with commercially approved balloon-expandable transcatheter heart valves (Sapien 3 and Ultra, Edwards Lifesciences, USA) and standard catheterization lab infrastructure.

研究设计

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

入排标准

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

入选标准

  • Patients aged ≥65
  • Indicated for transfemoral TAVR for severe aortic stenosis

排除标准

  • 未提供

研究组 & 干预措施

Use of tele-operated TAVIPILOT Software and Robot during the procedure

Experimental

TAVR procedure with TAVIPILOT Software and tele-operated robot by Caranx Medical enhancing the precision of transcatheter aortic valve positioning during TAVR.

干预措施: TAVR procedure with TAVIPILOT Software and tele-operated robot by Caranx Medical enhancing the precision of transcatheter aortic valve positioning during TAVR. (Device)

结局指标

主要结局

The investigational device-related safety will also be assessed by verifying the absence of major technical malfunctions

时间窗: Periprocedural

Investigational Device Safety

The primary objective is to evaluate investigational device-related safety, including the occurrence of investigational device-related conversion to open-heart surgery, investigational device-related valve embolization and investigational device-related.

时间窗: Periprocedural

Investigational device-related safety

次要结局

  • Device Performance(Periprocedural)
  • Clinician satisfaction(Periprocedural)

研究者

发起方
Caranx Medical
申办方类型
Industry
责任方
Sponsor

研究点 (2)

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