跳至主要内容
临床试验/NL-OMON30377
NL-OMON30377尚未招募不适用

Optimized convective volumes in postdilution HDF using ULTRACONTROL - Effect on blood purification efficacy - ULTRACONTROL HDF study

Gambro Lundia AB0 个研究点目标入组 10 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
10

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • 1 on dialysis since 3 months or longer
  • 2 stable on on-line postdilution HDF therapy since at least 1 month
  • 2a of which at least one week in ULTRACONTROL mode using Polyflux H dialyzer
  • 2b known on what total UF rate in relation to QB is possible during volume control mode when Polyflux H dialyzer is used, without having monitor TMP alarms
  • 3 regularly achieving a blood flow rate of 250 ml/min or more
  • 4 giving written consent to participate

排除标准

  • 1 Age <18 years
  • 2 Dialysis schedule other than 3 treatments per week
  • 3 Treatment time <3* or >5 hours
  • 4 Showing unstable blood flow rates and/or regularly showing access recirculation exceeding 5%.
  • 5 Treatments in single needle mode
  • 6 Expected to show poor compliance to dialysis prescription
  • 7 Known HIV, HBV, or HCV infection
  • 8 Known coagulation disorder
  • 9 Pregnant women, nursing mothers and women planning a pregnancy during the course of the study
  • 10 Patients under guardianship
  • 11 Participation in other studies that could interfere with the objectives of this study

研究者

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