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临床试验/IRCT20210620051631N1
IRCT20210620051631N1招募中3 期

Evaluation of the oral Nicorandil effect on reducing the contrast-induced nephropathy incidence in cardiac catheterization patients: a randomized controlled clinical trial

Mashhad University of Medical Sciences0 个研究点目标入组 344 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
入组人数
344

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 years 至 no limit(—)
性别
All

入选标准

  • Based on the risk score,Have a moderate risk or at least two risk factors for contrast nephropathy.
  • EF less than 40
  • Diabetes mellitus.
  • Blood pressure above 140/90 mm Hg,
  • Renal failure (GFR) less than 60
  • No pregnancy
  • (basal serum creatinine above 1.5 mg / dl)
  • Minimum age 18

排除标准

  • Pulmonary edema
  • Cardiogenic shock
  • Multiple myeloma
  • Acute renal failure
  • ESRD(GFR<15 mg/dl)
  • Allergy to media contrast
  • Nicorandil allergy
  • Facing media contrast in the last 7 days
  • NAC and metformin and dopamine and sodium bicarbonate and mannitol and phenol dopam in the last 48 hours

研究者

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