NCT01709487已完成1 期
Feasibility Study of Hyperthermic Intraperitoneal Chemotherapy (HIPEC) for Patients With Stage III or Only Pleural Stage IV Ovarian Carcinoma in First Line Therapy
适应症
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 19
- 试验地点
- 4
- 主要终点
- mortality rate
研究概览
简要总结
First line treatment for advanced ovarian carcinoma hyperthermic intraperitoneal chemotherapy (HIPEC) after optimal debulking.
详细描述
Addition of HIPEC to the standard first line treatment of ovarian carcinoma.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 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
- Female
- 接受健康志愿者
- 否
入选标准
- •stage III or only pleural stage IV ovarian carcinoma first line treatment
排除标准
- •incomplete surgery poor performance status bad general condition
结局指标
主要结局
mortality rate
时间窗: 24 weeks
We will record the mortality rate of our interventions: 3 cycles of pre-operative chemotherapy, surgery and HIPEC, 3 cycles of post-operative chemotherapy.
次要结局
- Overall survival(3 years)
- progression free survival(3 years)
研究者
研究点 (4)
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