跳至主要内容
临床试验/NCT00912366
NCT00912366终止不适用

A Prospective, Single Center, Observational Study Comparing the Safety and Efficacy of CVATS, HVATS and Open Surgery for Subjects Diagnosed With NSCLC Scheduled to Undergo a Lobectomy

Medtronic - MITG1 个研究点 分布在 1 个国家目标入组 39 人开始时间: 2009年5月最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
39
试验地点
1
主要终点
Assess hospital length of stay (LOS).

研究概览

简要总结

Assessment of VATS versus standard open surgery for treatment of non small cell lung cancer.

研究设计

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

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

  • Subject must be 18 years of age or older.
  • Subject must have been clinically diagnosed with stage I to stage IIA non small cell lung cancer measuring and judged to be resectable.
  • Subject must be able to tolerate general anesthesia, and have cardiopulmonary reserve to tolerate a lobectomy

排除标准

  • Subject is pregnant (documented by pregnancy test) or breastfeeding.
  • Subject has other severe illnesses that would preclude surgery such as
  • Unstable angina
  • Myocardial Infarction within 3 months
  • Coronary Artery Bypass Graft Surgery
  • Subject has other active cancers
  • Subject is unable to comply with any of the following:
  • Study requirements
  • Give valid informed consent
  • Follow-up schedule

结局指标

主要结局

Assess hospital length of stay (LOS).

时间窗: 1 time point (discharge)

Pain Scale Evaluation

时间窗: 5 time points out to 6 months

次要结局

  • Assess quality of life.(2 time points out to 6 months)
  • Assess peri-operative and post-operative complications.(5 time points out to 6 months.)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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