跳至主要内容
临床试验/NCT00157664
NCT00157664Unknown不适用

Canadian Longitudinal Thrombosis in End Stage Renal Disease Pilot Study

Hamilton Health Sciences Corporation1 个研究点 分布在 1 个国家目标入组 400 人开始时间: 2004年7月最近更新:
适应症

试验速览

阶段
不适用
入组人数
400
试验地点
1

研究概览

简要总结

The primary focus of this study is to collect information through diagnostic testing, blood sample analysis and patient data collection on patients starting hemodialysis to determine risk and preventative factors of bleeding and clotting events.

详细描述

Hemodialysis patients have a very high rate of heart attacks, strokes and amputation. These problems are caused by a blood vessel problem called atherosclerosis (hardening of the arteries), and by clotting. Clotting is also a problem in the access, which is their lifeline for hemodialysis. We have early results which show that some risk factors for clotting in the general population are common in dialysis patients. Bleeding is another significant problem within this population. In this pilot study we will measure bleeding/clotting factors in the blood of consenting patients who are just starting dialysis. We will also do special tests to show how much calcium build up and atherosclerotic build up has happened in the arteries and whether the arteries are becoming stiff. We will then follow patients for up to four years and record any health problems that might reflect bleeding, clotting or a blood vessel problem. At the end of the study, we will compare people who have had bleeding, clotting or blood vessel problem with those who have not, and learn which of the measurements predicted problems. We will go on to study potential treatments, such as anti-clotting drugs, which might prevent or delay the occurrence of such problems. This would improve the health of dialysis patients.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

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

  • Adult patient (aged > 18 years)
  • Patient on hemodialysis between 30 and 90 days

排除标准

  • Anticipated recovery of renal function (on dialysis < 90 days)
  • Critical illness at time of recruitment (patients who are critically ill [ICU] when first screened, who survive to 80 days, will be rescreened and will be able to participate at that point if no longer critically ill)
  • Planned live-donor renal transplant within 6 months
  • Patient cannot consent due to language barrier
  • Patient cannot consent due to cognitive difficulties
  • Patient cannot consent due to hearing impairment
  • Patient cannot consent due to speech impairment
  • Patient or decision maker declines consent
  • Patient is unable to give consent and no substitute decision maker is available
  • Patient on dialysis longer than 90 days

研究者

申办方类型
Other

研究点 (1)

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