Comparative Effectiveness of Bronchoscopic Interventions for Malignant Airway Obstruction
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 110
- 试验地点
- 1
- 主要终点
- Time to Any Complication Requiring Treatment
研究概览
简要总结
The goal of this clinical research study is learn about side effects and the success of bronchoscopies when performed in cancer patients with and without symptoms.
This is an investigational study.
Up to 110 patients will take part in this study. All will be enrolled at MD Anderson.
详细描述
If participant agrees to take part in this study, researchers will collect information from participant's medical records.
Length of Study:
Researchers will continue to collect participant's medical information for up to 2 years.
Additional Information:
Participant's data will be kept in a database on a password-protected computer in a secure office. This information will only be available to the study doctors and staff.
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
- •° All patients undergoing interventional bronchoscopy during the first 12 months will be enrolled, with follow-up occurring out to 2 years from the study startup (the duration of the grant).
排除标准
- •Age less than 18 years,
- •Inability to participate in telephone follow-up
结局指标
主要结局
Time to Any Complication Requiring Treatment
时间窗: 2 years
Researchers will estimate the hazard function of time to any complications in the framework of competing risks while death is the competing risk.3 Researchers will graphically visualize the hazard function of time to any complications using Kernel smoothing method.
次要结局
- Quality-Adjusted Survival(2 years)