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
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
- 否
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
研究点 (1)
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