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临床试验/NL-OMON52060
NL-OMON52060招募中4 期

Goal directed fluid removal with furosemide in intensive care patients with fluid overload - A randomised, blinded, placebo-controlled trial - GODIF

ordsjaellands Hospital, University of Copenhagen0 个研究点目标入组 100 人开始时间: 待定最近更新:
适应症

试验速览

阶段
4 期
状态
招募中
发起方
入组人数
100

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • All of the following criteria must be fulfilled:
  • Acute admission to the Intensive Care Unit.
  • Age >= 18 years of age.
  • Fluid overload defined as a positive cumulative fluid balance (according to
  • the daily fluid charts) corresponding >= 5 % of ideal body weight (calculated
  • as: 22 x (height in meters)^2). If possible, all fluids administered before
  • admission to the ICU are to be included in the calculation of cumulative fluid
  • Clinical stable defined as Mean Arterial Pressure > 50 mmHg and maximum
  • infusion of 0.20 microgram/kg/minute of noradrenaline and lactate < 4.0 mmol/L.

排除标准

  • Known allergy to furosemide or sulphonamides.
  • Known pre-hospitalisation advanced chronic kidney disease (eGFR < 30
  • mL/minute/1.73 m2 or chronic RRT).
  • Ongoing RRT.
  • Anuria for >= 6 hours.
  • Rhabdomyolysis with indication for forced diuresis
  • Ongoing life-threatening bleeding as these patients need specific fluid/blood
  • product strategies.
  • Acute burn injury of more than 10 % of the body surface area as these
  • patients need a specific fluid strategy.
  • Severe dysnatraemia (p-Na < 120 or > 155 mmol/l) as these patients need a
  • specific fluid strategy.
  • Severe hepatic failure as per the clinical team.
  • Patients undergoing forced treatment.
  • Fertile women (women < 50 years) with positive urine human chorionic
  • gonadotropin (hCG) or plasma-hCG.
  • Consent not obtainable as per the model approved for the specific trial site.

研究者

发起方
ordsjaellands Hospital, University of Copenhagen

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