NCT00259584已完成1 期
A Prospective Longitudinal Study of the Management and Outcome of Superior Vena Caval Obstruction (SVCO)
适应症
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 20
- 试验地点
- 1
- 主要终点
- Improvement in an index symptom at 4 weeks as recorded by a daily symptom diary
研究概览
简要总结
All patients with symptomatic malignant SVCO deemed suitable for treatment either with radiation therapy or by stenting will be eligible. They will receive whichever treatment is deemed most clinically appropriate. Symptomatic response, time to onset of palliation, duration of symptom control and survival will be assessed.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
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
- •Symptomatic clinical and radiological diagnosis of superior vena caval obstruction.
- •Underlying histological diagnosis deemed appropriate for palliative radiotherapy as treatment by investigator. Patients with chemosensitive tumours such as small cell lung cancer (both untreated and recurrent), lymphoma and testicular tumours, will be eligible if radiation is deemed to be appropriate treatment.
排除标准
- 未提供
结局指标
主要结局
Improvement in an index symptom at 4 weeks as recorded by a daily symptom diary
次要结局
- Time to onset of palliation
- Duration of symptom control
- Survival
- Number of days spent in hospital
- Requirement for further treatment
研究者
研究点 (1)
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