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临床试验/NCT01221337
NCT01221337已完成不适用

Comparative Study of Two Haemodialyzers "VIE 2.1" Versus "EVODIAL2.2" in a Strategy of Heparin-free Haemodialysis (HFH)

Centre Hospitalier Universitaire de Nice2 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2010年10月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
32
试验地点
2
主要终点
The percentage of successful study periods with no circuit-clotting event leading to a premature interruption of any of the four dialysis sessions

研究概览

简要总结

The adequate anti coagulation is an absolute necessity in order to avoid the extra-corporal circuit and haemodialyzer clotting and to perform an adequate renal replacement therapy during a haemodialysis session. In the cases of multiple coagulation defects having high haemorrhagic risk factors and the patients under anti-coagulation therapy, it is recommended to reduce the heparin doses or to do heparin free haemodialysis. Several strategies of low heparin or heparin free haemodialysis have been proposed till now, without a real success. The heparin coated polyacrylonitrile haemodialyser (EVODIAL) has been reported to have 90 % successful heparin-free haemodialysis sessions. On the other hand, the vitamin E coated polysulphone (VIE) has also been reported to have an anti oxidative and anti-thrombotic properties and a capacity to improve the haemorrheological factors of human blood, hence having a promising future to perform a successful haemodialysis session with less or without heparin. This randomised, multi-centric, cross-over and open study has been designed to compare non inferiority of the haemodialyzer VIE 2,1 versus EVODIAL2,2 with a risk alfa of 5% and an absolute accepted difference of 12 %.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Prevention
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

  • •- Adult chronic haemodialysis patients since al least 3 months
  • •Two needles puncture of the fistula,
  • •Low molecular weight heparinization during haemodialysis sessions,
  • •Good fistula or central veinous catheter flow rate (blood pump flow rate ≥ 300 ml/min),
  • •Systolic blood pressure ≥ 110 mmHg (mean value of three last dialysis sessions.
  • •Patients capable to understand the design of the study and to follow the instructions
  • •Patients having the French social security system affiliation.
  • •Non-inclusion criteria :
  • •C reactive protein > 30 mg/L.
  • •Single needle puncture of the fistula
  • •Active documented haemorrhage,
  • •Haemoglobin < 10 g/dl and/or need blood transfusion,
  • •Documented thrombophilia
  • •Patients waiting for renal graft
  • •Acute sepsis
  • •Fistula or catheter dysfunction
  • •Patients under anti-vitamine K
  • •Per dialytic hypotension requiring al least once a nurse intervention,
  • •Severe diseases (Dysglobulinemia, vascularitis, HIV...),
  • •Patients following another research protocol or have ended one less then one month before starting of this study.
  • •Pregnant or breast feeding patients,
  • •Minor patients or under law-protection

排除标准

  • 未提供

研究组 & 干预措施

haemodialyzer EVODIAL-haemodialyzer VIE

Other

Equal number of patients will start either with the haemodialyzer "VIE 2,1" or "EVODIAL 2,2" followed by a wash out period, before starting the other haemodialyzer.

干预措施: heparin free haemodialysis (Other)

haemodialyzer VIE-haemodialyzer Evodial

Other

Equal number of patients will start either with the haemodialyzer "VIE 2,1" or "EVODIAL 2,2" followed by a wash out period, before starting the other haemodialyzer.

干预措施: heparin free haemodialysis (Other)

结局指标

主要结局

The percentage of successful study periods with no circuit-clotting event leading to a premature interruption of any of the four dialysis sessions

时间窗: during every haemodialysis sessions

次要结局

  • Duration of dialysis session without blood circuit clotting(during every haemodialysis sessions)
  • Number of times saline rinsing has been required(during every haemodialysis)
  • Degree of blood clots in the venous bubble trap(during every haemodialysis sessions)
  • Quality of blood restitution(during every haemodialysis sessions)
  • Dialysis adequacy (KT/V)(during every haemodialysis sessions)
  • Haematological status(during every haemodialysis sessions)
  • tolerance(during every haemodialysis sessions)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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