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临床试验/NCT01414842
NCT01414842已完成4 期

Randomized Controlled Study on the Effect of the Hemodiafiltration Plasma Sodium Biofeedback System on Cardiovascular Stability in Hemodialysis Patients

Azienda Ospedaliera di Lecco12 个研究点 分布在 5 个国家目标入组 50 人开始时间: 2007年4月1日最近更新:
适应症
干预措施

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
50
试验地点
12
主要终点
Number of dialysis complicated by at least one hypotension

研究概览

简要总结

Aim of the present randomized controlled multinational trial is the comparison of a novel biofeedback system on sodium profiling applied to a endogenous hemodiafiltration therapy, with the standard (no sodium profiling) hemodiafiltration technique on the intradialytic overall and cardiovascular stability.

详细描述

Online hemodiafiltration (OL-HDF) has been recently associated with better patient survival in comparison with standard hemodialysis in some large observational studies (Canaud et al, KI, 2006; Vilar et al, CJASN , 2009) supporting the hypothesis that convection can improve patients outcomes. Moreover, it has been demonstrated in randomized controlled trials (Locatelli et al, Journal American Society of Nephrology, 2010) that OL-HDF significantly reduced the frequency of intradialytic hypotension. Nonetheless, the associated comorbidities and ageing of dialysis population require further devices able to improve treatment tolerance. Among these tools, the sodium profiling and biofeedback system seem to be promising to accomplish this task. But the correct intradialytic sodium balance is still far away today to be easily achieved. The use of an automated adaptive system dialysis to the sodium profiling has been investigated in a feasibility trial (Colì et al International Journal Artificial Organs, 2003). They also investigated the impact of such a device on treatment tolerance.

The aim of this randomized multinational multicenter controlled trial is to evaluate the impact of sodium profiling applied to a endogenous hemodiafiltration technique on the intradialytic cardiovascular stability in comparison to standard no profiled endogenous hemodiafiltration.

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 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients with more than 30% of dialysis complicated by hypotension
  • •age between 18 and 85 yers
  • •time on dialysis greater than 6 months
  • •residual creatinine clearance less than 2 ml/min/1.73 m2
  • •native fistula or central venous catheter with blood flow rate greater than 250 ml/min

排除标准

  • •Life expectancy less than 1 year
  • •solid active neoplasm
  • •pregnancy
  • •major event in the previous 3 months (ictus, myocardial infarction, cachexia)

研究组 & 干预措施

Standard

Active Comparator

Standard constant (no profiled) sodium dialysate used during endogenous hemodiafiltration

干预措施: Standard sodium dialysate (Device)

Automated profiled

Experimental

Automate sodium profiling in endogenous hemodiafiltration

干预措施: Automated sodium profiling in endogenous hemodiafiltration (Device)

结局指标

主要结局

Number of dialysis complicated by at least one hypotension

时间窗: six months

Hypotension definition: If predialysis systolic blood pressure greater than100 mmHg then a value during dialysis below 90 mmHg or any systolic blood pressure reduction greater than 25 mmHg in presence of symptoms or If predialysis systolic blood pressure less than 90 mmHg a reduction of at least 10% accompanied by symptoms

次要结局

  • Blood Pressure Intradialytic symptoms(six months)

研究者

发起方
Azienda Ospedaliera di Lecco
申办方类型
Other
责任方
Principal Investigator
主要研究者

Francesco Locatelli

Prof.

Azienda Ospedaliera di Lecco

研究点 (12)

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