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临床试验/ISRCTN42955626
ISRCTN42955626
已完成
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Accuracy of glomerular filtration rate (GFR) estimation using creatinine and cystatin C and albuminuria for monitoring disease progression in patients with stage 3 chronic kidney disease - prospective longitudinal study in a multi-ethnic population: the eGFR-C study

niversity of Birmingham (UK)0 个研究点目标入组 1,320 人2013年10月8日

概览

阶段
未知
干预措施
未指定
疾病 / 适应症
Topic: Renal and Urogenital
发起方
niversity of Birmingham (UK)
入组人数
1320
状态
已完成
最后更新
去年

概览

简要总结

2014 Protocol article in http://www.ncbi.nlm.nih.gov/pubmed/24423077 2019 Results article in https://pubmed.ncbi.nlm.nih.gov/31084924/ (added 10/08/2020) 2024 Results article in https://pubmed.ncbi.nlm.nih.gov/39056437/ (added 29/07/2024)

注册库
who.int
开始日期
2013年10月8日
结束日期
2020年6月30日
最后更新
去年
研究类型
Observational
性别
All

研究者

发起方
niversity of Birmingham (UK)

入排标准

入选标准

  • 1\. Male and female, aged 18 years or over
  • 2\. Patients with stage 3 CKD (GFR 30\-59 mL/min/1\.73 m2\) as defined internationally, diagnosed using Modification of Diet in Renal Disease/Chronic Kidney Disease Epidemiology Collaboration (MDRD/CKD EPI) eGFR (at least two consecutive test results in this range at least 90 days apart, with the most recent test in the last 12 months)
  • 3\. Written informed consent

排除标准

  • 1\. History of untoward reactions to iodinated contrast media or allergy to topical iodine
  • 2\. Episode of acute kidney injury in previous 6 months (as defined by the Acute Kidney Injury Network criteria)
  • 3\. Amputation of whole or part limb
  • 4\. Pregnant or breastfeeding
  • 5\. Known alcohol or drug abuse
  • 6\. Any clinical condition with an expected survival of less than study duration
  • 7\. Inability to comply with study schedule and follow\-up
  • 8\. Inability to provide informed consent e.g. due to cognitive impairment

结局指标

主要结局

未指定

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