跳至主要内容
临床试验/NL-OMON53024
NL-OMON53024招募中不适用

Renoprotective effects of potassium supplementation in chronic kidney disease - K+ in CKD

Erasmus MC, Universitair Medisch Centrum Rotterdam0 个研究点目标入组 532 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
532

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

  • - Adult patients with CKD stage 3b or 4
  • - Fall in eGFR > 2 ml/min/1.73 m2/year in preceding years
  • - Hypertension (automated blood pressure > 140/90 mmHg or use of
  • anti-hypertensive medication)

排除标准

  • - Hyperkalemia (serum potassium > 5.5 mmol/l) at study visit V0
  • - Medical reasons to continue dual RAAS-blockade, mineralocorticoid receptor
  • blockers, potassium-sparing diuretics, or oral potassium binders.
  • - Patients using calcineurin inhibitors
  • - Patients using tolvaptan
  • - Kidney transplant recipients
  • - Patients with an active gastro-intestinal ulcus
  • - Patients with previous history of ventricular cardiac arrhythmia
  • - Patients with a life expectancy < 6 months
  • - Expected initiation of renal replacement therapy < 2 years
  • - Incapacitated subjects or subjects who are deemed unfit to adequately adhere
  • to instructions from the research team
  • - Women who are pregnant, breastfeeding or consider pregnancy in the coming 2

研究者

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