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临床试验/NCT02499185
NCT02499185终止4 期

A PILOT Study Evaluating Novel Biomarkers of AKI in Post-operative Patients Undergoing Major Intra-Abdominal Surgery

Universitair Ziekenhuis Brussel2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2015年4月1日最近更新:
适应症
干预措施

试验速览

阶段
4 期
状态
终止
入组人数
100
试验地点
2
主要终点
Number of participants diagnosed with AKI stage 2 or 3 using the updated rifle "KDIGO" guidelines

研究概览

简要总结

To validate the use of [TIMP-2]●[IGFBP-7] to predict AKI in patients undergoing major intra abdominal surgery.

详细描述

A prospective pilot single center study to investigate the potential of [TIMP-2].[IGFBP-7] to predict AKI (Acute Kidney Injury) in patients undergoing major abdominal surgery. The investigators will measure the biomarker once preoperatively and 4-times postoperatively starting at arrival on PACU (post anesthesia care unit).The primary endpoint of this study is the development of AKI stage 2 or 3 within the first 72 postoperative hours.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Diagnostic
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

  • ≥ 18 years
  • High risk patients: General Surgery AKI Risk Index Class III, IV or V
  • Major abdominal surgery

排除标准

  • Ongoing acute kidney injury Stage 2/3
  • History of kidney transplant

研究组 & 干预措施

Nephro Check Test

Experimental

We take urine samples and analyse the level of [TIMP-2]●[IGFBP-7] using the NephroCheck Test to diagnose AKI

干预措施: Nephro Check Test (Device)

Nephro Check Test

Experimental

We take urine samples and analyse the level of [TIMP-2]●[IGFBP-7] using the NephroCheck Test to diagnose AKI

干预措施: serum creatinine measurement (Other)

serum creatinine measurement

Active Comparator

This is the "Golden standard" to diagnose AKI

干预措施: Nephro Check Test (Device)

serum creatinine measurement

Active Comparator

This is the "Golden standard" to diagnose AKI

干预措施: serum creatinine measurement (Other)

结局指标

主要结局

Number of participants diagnosed with AKI stage 2 or 3 using the updated rifle "KDIGO" guidelines

时间窗: 72 Hours

次要结局

  • Number of participants who need renal replacement therapy(30 Days)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Veerle Van Mossevelde

Data Nurse

Universitair Ziekenhuis Brussel

研究点 (2)

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