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临床试验/NCT04551391
NCT04551391已完成不适用

Kidney Recovery After Acute Kidney Injury - Longitudinal Study

NHS Lothian1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2020年1月7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
NHS Lothian
入组人数
100
试验地点
1
主要终点
To primary outcome aims to measure whether circulating ET is higher in patients with AKI than in matched controls.

研究概览

简要总结

The endothelin (ET) system is an active target in human Acute Kidney Injury (AKI).

Our primary hypothesis is that the circulating blood concentration of ET will be higher in patients with AKI than in matched controls.

详细描述

Acute kidney injury (AKI) is a major health problem being both common and costly. It affects ~20% of hospital inpatients and consumes ~1% of the annual NHS budget. AKI occurs following a diverse range of insults, commonly ischaemia-reperfusion injury (IRI) but also sepsis and drug toxicity. Therapies for AKI are currently supportive and short-term mortality remains high, with ~2 million deaths per year worldwide. In those who survive an episode of AKI, 30% are left with chronic kidney disease (CKD). The remaining 70% that recover full renal function are at ~28-fold increased risk of ultimately developing CKD. This risk is even greater in elderly patients. Importantly, CKD is strongly and independently associated with incident cardiovascular disease (CVD), and together these exert a global socioeconomic burden.

The recognition that AKI and CKD are linked is recent and the molecular pathways that control the transition from acute injury to chronic disease are not well defined. Currently, there are no specific treatments that reduce the risk of progressing to CKD after AKI. Thus, there is an unmet need for therapies that will prevent the transition from AKI to CKD and reduce the cardiovascular burden associated with both. Our preliminary investigations (not yet published) in humans and mice suggest that AKI causes sustained activation of the endothelin (ET) system to the long-term detriment of renal and systemic haemodynamic function. These pilot data form the basis of our project that seeks to determine whether the ET system is active in patients with AKI and, thus, represents a potential target for therapeutic intervention.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

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

入选标准

  • (i) Adult aged 16 or over; (ii) Ability to provide informed consent; (iii) Diagnosis of AKI determined as:
  • Previous (within 3 years) eGFR >45 mL/min/1.73m2 OR no history of kidney disease if no recent (within 3 years) blood results available AND
  • Elevated creatinine over 1.5 x previous result OR over 150 μmol/L if no previous value AND
  • Increasing creatinine >= 27μmol/L above index value within 48 hours
  • The control group (N=50) inclusion criteria are:
  • (i) Adult aged 16 or over; (ii) Ability to provide informed consent; (iii) Admitted to hospital without AKI: (eGFR > 60)
  • This group will be recruited contemporaneously with, and matched to, AKI participants by:
  • Age (± 5 years)
  • AKI aetiology (ischaemic, infected, nephrotoxic) 4 (i) History of diabetes or not AND/OR (ii) History of cardiovascular disease or not

排除标准

  • Inability to provide informed consent
  • Pregnancy or breast feeding
  • Evidence of CKD

结局指标

主要结局

To primary outcome aims to measure whether circulating ET is higher in patients with AKI than in matched controls.

时间窗: 3 years

as above

次要结局

  • The secondary outcome aims to measure differences in urine ET between patients with AKI and matched controls AKI patients that do not fully recover renal function within 90 days will have the highest concentrations of blood and urine ET.(3 YEARS)

研究者

发起方
NHS Lothian
申办方类型
Other Gov
责任方
Sponsor

研究点 (1)

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