跳至主要内容
临床试验/NCT00303420
NCT00303420终止4 期

Alteplase for Blood Flow Restoration in Hemodialysis Catheters: A Randomized Prospective Clinical Trial

University of Manitoba9 个研究点 分布在 1 个国家目标入组 180 人开始时间: 2004年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
终止
入组人数
180
试验地点
9
主要终点
Proportion of patients with pre-thrombolytic blood flows less than 200 ml/min achieving a "sustainable" post thrombolytic blood flow > or = 300 ml/min.

研究概览

简要总结

We are investigating a new way of administering alteplase to remove clots from hemodialysis catheters. Currently, alteplase is left to dwell inside the catheter between dialysis treatments to dissolve the clot and restore blood flow through the catheter. We have developed a new way to administer alteplase by advancing it to the tip of the catheter at regular 10 minute intervals. We hypothesize that our new "push" protocol will dissolve clots in hemodialysis catheters better and faster than the current dwell method.

详细描述

Central venous catheters are commonly used for vascular access in the hemodialysis population. A common complication is low / no blood flow through the catheter due to clots. These are serious situations because patients may miss dialysis sessions and suffer significant morbidity. In an attempt to dissolve the clots and restore blood flow, thrombolytics are frequently instilled into the catheters between dialysis sessions . However, we have developed and new "push" protocol that advances fresh thrombolytic (alteplase) to the tip of the catheter in order to facilitate more effective and faster removal of the clot. We hypothesize that our new "push" protocol will dissolve clots in hemodialysis catheters better and faster than the current dwell method.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
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

入选标准

  • Adults > 18 yrs old
  • Hemodialysis patients
  • Vascular access with a permanent catheter
  • No prior rt-PA use in the catheter over the previous 21 days
  • One rt-PA instillation per catheter (i.e. we will only document the results of 1 rt-PA instillation per catheter. Numerous rt-PA instillations in the same catheter will NOT be considered new events, and not entered into the study)

排除标准

  • Critically ill patients in the ICU setting.
  • Contraindications / cautions with alteplase use including: known hypersensitivity to alteplase or its components (l-arginine, phosphoric acid, polysorbate 80), patients with known conditions associated with bleeding events (e.g.intracranial bleed in last 4 weeks, major hemorrhage in last 4 weeks (Hgb drop of 20 g/L)), recent surgery (<48 hours), recent biopsy (<48 hours), hemostatic defects including severe hepatic disease, or current intracranial / intraspinal neoplasm.
  • Hemodialysis catheter has been in the patient less than 14 days.

研究组 & 干预措施

1

Active Comparator

Alteplase used by normal dwell procedure

干预措施: alteplase dwell arm (Drug)

2

Experimental

Alteplase given by an new "push" protocol

干预措施: Alteplase "push" protocol (Drug)

结局指标

主要结局

Proportion of patients with pre-thrombolytic blood flows less than 200 ml/min achieving a "sustainable" post thrombolytic blood flow > or = 300 ml/min.

时间窗: 4 hours

次要结局

  • Highest recorded "sustainable" blood flow (ml/min) pre- and post- thrombolytic administration.(4 hours)
  • Change in Kt/V from the treatment before thrombolytic administration compared to the treatment after thrombolytic administration.(72 hours)
  • Change in "litres processed / time" from the treatment before thrombolytic administration compared to the treatment after thrombolytic administration.(72 hours)
  • Serious adverse events including major bleeding within 24 hours of alteplase administration(30 days post-last dose)

研究者

申办方类型
Other

研究点 (9)

Loading locations...

相似试验