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临床试验/NCT06471777
NCT06471777尚未招募不适用

Proactive Prescription-based Fluid Management Versus Usual Care in Critically Ill Patients on Kidney Replacement Therapy Trial in UK

Guy's and St Thomas' NHS Foundation Trust0 个研究点目标入组 20 人开始时间: 2024年8月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
20
主要终点
fluid balance

研究概览

简要总结

The PROBE Fluid UK randomised controlled trial compares a protocol-based fluid removal strategy with usual care in critically ill patients with acute kidney injury receiving kidney replacement therapy.

详细描述

Severe acute kidney injury (AKI) in the intensive care unit (ICU) is almost uniformly complicated by fluid accumulation, often leading to fluid overload. Congestion resulting from fluid accumulation is believed to contribute to organ failure. Removal of excess fluid is a central component of dialysis treatment, also known as kidney replacement therapy (KRT). However, there remain important knowledge gaps in our ability to remove excess fluid effectively and safely. If fluid is removed too slowly, fluid overload and its complications persist for longer. If fluid is removed too fast during KRT, patient's blood pressure may drop (ie hemodynamic instability may occur) which may precipitate complications.

The optimal fluid management strategy is currently unknown.

The PROBE Fluid UK study is a randomized clinical trial comparing a protocol-based fluid removal strategy with usual care in critically ill patients with AKI receiving KRT. The fluid management protocol is intended to achieve neutral or negative daily fluid balance by both preventing and treating fluid accumulation.

The primary objective of this trial is to determine whether the intervention results in a difference in cumulative fluid balance from day of randomization to 5 days later. Secondary outcomes will include short-term patient outcomes, safety outcomes, and health resource utilization related to KRT delivery.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
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

  • Adult patients aged ≥18 years
  • Admitted to the intensive care unit
  • Acute kidney injury defined by the KDIGO criteria
  • Planned initiation of KRT within 12 hours or the receipt of KRT for AKI for ≤48 hours

排除标准

  • Lack of commitment to maintain kidney, pharmacologic or respiratory support at the time of screening, or probable transition to comfort care within 48 hours according to the treating clinician
  • Probable discharge from the ICU within 48 hours according to treating clinician
  • Severe burn injury (>10% of body surface area)
  • Severe abnormality in serum sodium (>155 or <120 mmol/L)
  • Important ongoing fluid losses are present and/or are expected to require continued maintenance IV fluids during the next 48 hours
  • The clinical care team believes that the proposed intervention is inappropriate

结局指标

主要结局

fluid balance

时间窗: day 5 after randomization

cumulative fluid balance

次要结局

  • ICU stay(90 days after randomization)
  • enrolment(20 months)
  • mechanical ventilation(28 days after randomization)
  • mortality(90 days after randomization)
  • vasoactive therapy(28 days after randomization)
  • KRT duration(5 days)

研究者

申办方类型
Other
责任方
Sponsor

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