NCT00752583已完成不适用
Clinical Study in Order to Quantify Solute Removal in Peritoneal Dialysis Versus Haemodialysis
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 25
- 试验地点
- 2
- 主要终点
- Registration of toxin removal efficiency
研究概览
简要总结
Study in order to quantify toxin removal during dialysis
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 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
- •Substudy 1: includes new starting dialysis patients on peritoneal dialysis PD or haemodialysis HD
- •Substudy 2: stabile haemodialysis patients and peritoneal dialysis patients. Patients will be matched for gender, time on dialysis, diabetes, renal function at the start of dialysis.
- •Substudy 3: patients on CAPD (continuous ambulant PD) or CCPD (continuous cyclic PD).
排除标准
- 未提供
结局指标
主要结局
Registration of toxin removal efficiency
时间窗: After 1 week and after 1, 3, 6, 9, 12, 18 and 24 months
次要结局
未报告次要终点
研究者
研究点 (2)
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