跳至主要内容
临床试验/NCT01405092
NCT01405092已完成不适用

Continuous Versus Conventional Volume Management During CRRT (Continuous Renal Replacement Therapy)

Dallas VA Medical Center2 个研究点 分布在 1 个国家目标入组 28 人开始时间: 2010年4月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
28
试验地点
2
主要终点
compare number of hypotensive events in treatment versus control arms

研究概览

简要总结

Use of on-line blood volume monitoring during continuous renal replacement therapy can improve volume management in acute kidney injury patients requiring renal replacement

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
21 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with kidney injury requiring continuous renal replacement therapy and volume removal

排除标准

  • unable to provide or obtain patient consent
  • not expected to survive 48 hours

结局指标

主要结局

compare number of hypotensive events in treatment versus control arms

时间窗: 24 hour for each arm

compare the number of hypotensive events during use of crit-line monitor over 24 hour period versus during control 24 hour period

次要结局

未报告次要终点

研究者

申办方类型
Fed
责任方
Principal Investigator
主要研究者

Devasmita C. Dev MD

Director of In-center and Home Dialysis

Dallas VA Medical Center

研究点 (2)

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