NCT02356822撤回不适用
Sarah Cannon Outcomes Registry
适应症
试验速览
- 阶段
- 不适用
- 状态
- 撤回
- 试验地点
- 1
- 主要终点
- quality improvement
研究概览
简要总结
This is an investigational multi-site outcomes registry intended to collect information about a patient's cancer care. Patients may enter the Registry at any time during the patient's current stage in the continuum of care. The registries main objectives will be to measure and evaluate the effects of patient care throughout the care continuum, resulting in the identification of the most effective treatment options. Objectives will encompass evaluations and analytics around safety, effectiveness, and improved efficiencies.
详细描述
Q
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Other
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
- •18 or older
- •Patients that have been diagnosed with/ or are thought to have any form of cancer at any stage in the continuum of their care from screening through survivorship.
- •Patient must have the ability to understand the nature of the trial and give written informed consent
排除标准
- •There are no exclusion criteria for this Outcomes Registry
结局指标
主要结局
quality improvement
时间窗: 10 yrs
Treatment patterns and utilization
时间窗: 5 yrs
次要结局
- Humanistic and economic outcomes(10 yrs)
研究者
研究点 (1)
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