ISRCTN42955626
已完成
未知
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)
研究者
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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