跳至主要内容
临床试验/NCT06952894
NCT06952894已完成不适用

Feasibility and Efficacy of Surgical Navigation 'RUS Lung' in Patients Undergoing Minimally Invasive Thoracic Surgery (MITS) Segmentectomy for Lung Cancer: a Multicenter Prospective Observational Study With a Propensity-score Matching Analysis

Hutom Corp1 个研究点 分布在 1 个国家目标入组 34 人开始时间: 2025年5月12日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
34
试验地点
1
主要终点
The concordance rate of tumor location across CT, RUS Lung, and surgery

研究概览

简要总结

This sponsor-initiated prospective observational study aims to demonstrate the feasibility and efficacy of RUS Lung Surgical Navigation System in patients undergoing minimally invasive thoracic surgery(MITS). The trial will enroll 36 patients who undergo video-assisted or robot-assisted thoracoscopic surgery using RUS Lung. The study will be conducted across two medical centers."

  • Investigational Medical Device: RUS Lung (Endoscopic Imaging Treatment Planning Software)
  • Clinical Trial duration: 12 months from IRB approval
  • Target number of subjects: Total of 36 participants

详细描述

Patients will be enrolled after being selected based on the inclusion and exclusion criteria and after obtaining informed consent. Video-assisted or robot-assisted thoracic surgery (VATS/RATS) will be performed using RUS Lung.Parameters-associated with operation or clinical outcomes will be evaluated during hospitalization period or through outpatient follow-ups for up to 2 weeks after discharge. The operative outcomes including operative time, estimated blood loss, complication rates, and hospital length were compared with the historical control underwent VATS and RATS without using RUS Lung.

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
19 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Individuals who were diagnosed with lung caner (tumor size≤3cm)
  • Individuals aged 19 or older
  • Individuals who who are able to undergo CT imaging according to the established protocol
  • Individuals who have voluntarily given written consent to participate in this clinical trial

排除标准

  • Vulnerable subjects
  • Individuals who who are not able to undergo CT imaging according to the established protocol
  • Individuals who are expected to have severe adhesions
  • Individuals who are unable to follow the study procedures and are deemed inappropriate for participation

结局指标

主要结局

The concordance rate of tumor location across CT, RUS Lung, and surgery

时间窗: The operative day (operative day ± 5 days)

Overall feasibility of the RUS Lung system will be evaluated by 3 factors as below. 1. CT turn-around time: the duration between uploading of preoperative CT and downloading the 3D model file 2. The stability of the RUS Lung system 3. The concordance rate of tumor location across CT, RUS Lung, and surgery

次要结局

  • The degree of consistency between surgical planning using the RUS lung system and actual surgical findings.(From enrollment to the end of treatment at 2 weeks)

研究者

发起方
Hutom Corp
申办方类型
Industry
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验