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临床试验/NCT06037109
NCT06037109已完成不适用

VIDAS® NEPHROCLEAR CCL14 Reference Interval Study

BioMérieux2 个研究点 分布在 1 个国家目标入组 585 人开始时间: 2023年7月18日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
BioMérieux
入组人数
585
试验地点
2
主要终点
CCL14 concentration in urine

研究概览

简要总结

This is a multi-center sample analysis study in which urine samples previously collected from apparently healthy adult subjects, and subjects with stable chronic morbidities but without AKI in order to establish the reference range for the VIDAS® NEPHROCLEAR™ CCL14 test.

详细描述

The VIDAS® NEPHROCLEAR™ CCL14 Test is intended to be used in conjunction with clinical evaluation, in ICU patients with moderate to severe (stage 2 or 3) acute kidney injury (AKI), as an aid in the risk assessment for developing persistent severe AKI (stage 3 AKI lasting ≥ 72 hours) within 48 hours of patient assessment.

The VIDAS® NEPHROCLEAR™ CCL14 Test is intended to be used in patients 21 years of age or older.

The objective of this study is to determine the reference range for CCL14 concentration in Apparently Healthy Adults and Adults with Chronic, Stable Morbidities

研究设计

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

入排标准

年龄范围
21 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Apparently healthy adults (age ≥ 21 years);
  • Provide written informed consent for study (AST-017) participation

排除标准

  • Any known or suspected acute illness or condition - including acute infections - at the time of enrollment or within the previous 30 days;
  • Any known or suspected significant new onset or chronic morbid medical condition such as:
  • Active cancer
  • Arrhythmia (atrial fibrillation, heart block, ventricular tachycardia)
  • Chronic coagulation abnormality
  • Chronic obstructive pulmonary disease (including emphysema, chronic bronchitis, and asthma)
  • Chronic pancreatitis
  • Chronic renal insufficiency
  • Congestive heart failure
  • Coronary artery disease
  • Diabetes mellitus (Type 1 or Type 2)
  • Hyper- or hypothyroidism
  • Hyperlipidemia (includes hypercholesterolemia)
  • Hypertension
  • Immunocompromised
  • Inflammatory bowel disease (including Crohn's disease and ulcerative colitis)
  • Liver cirrhosis
  • Neuromuscular disease
  • Peripheral vascular disease (a.k.a. peripheral artery disease)
  • Polycystic kidney disease
  • Rheumatoid arthritis
  • Systemic Lupus Erythematosus
  • Trauma-related surgery within the last 6 months;
  • Any surgery, hospitalization or institutionalization (such as in a nursing home) during the previous 3 months;
  • Received any blood product transfusion within the previous 2 months;
  • Pregnant women or children;
  • Prisoners or institutionalized individuals;
  • Already provided a urine sample for the AST-017 study
  • Inclusion Criteria:
  • Adults (age ≥ 21 years);
  • One or more of the following chronic, stable morbid conditions:
  • Active cancer
  • Arrhythmia (atrial fibrillation, heart block, ventricular tachycardia)
  • Chronic coagulation abnormality
  • Chronic obstructive pulmonary disease (including emphysema, chronic bronchitis, and asthma)
  • Chronic pancreatitis
  • Chronic renal insufficiency
  • Congestive heart failure
  • Coronary artery disease
  • Diabetes mellitus (Type 1 or Type 2)
  • Hyper- or hypothyroidism
  • Hyperlipidemia (includes hypercholesterolemia)
  • Hypertension
  • Immunocompromised
  • Inflammatory bowel disease (including Crohn's disease and ulcerative colitis)
  • Liver cirrhosis
  • Neuromuscular disease
  • Peripheral vascular disease (a.k.a. peripheral artery disease)
  • Polycystic kidney disease
  • Rheumatoid arthritis
  • 另有 15 项未显示

结局指标

主要结局

CCL14 concentration in urine

时间窗: Samples tested within 2 years of collection

CCL14 concentration will be measured using the VIDAS Necphroclear CCL14 Assay

次要结局

未报告次要终点

研究者

发起方
BioMérieux
申办方类型
Industry
责任方
Sponsor

研究点 (2)

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