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临床试验/PER-055-16
PER-055-16已完成未知

A STUDY TO EVALUATE THE EFFECT OF DAPAGLIFLOZIN ON RENAL OUTCOMES AND CARDIOVASCULAR MORTALITY IN PATIENTS WITH CHRONIC KIDNEY DISEASE

ASTRAZENECA PERU S.A.,0 个研究点目标入组 218 人开始时间: 2017年5月17日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
218

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

性别
All

入选标准

  • 1. Provision of signed informed consent prior to any study specific procedures
  • 2. Female or male aged ≥18 years at the time of consent
  • 3. eGFR ≥25 and ≤75 mL/min/1.73m2 (CKD-EPI Formula) at visit 1
  • 4. UACR ≥200 and ≤5000 mg/g at visit 1
  • 5. Stable, and for the patient maximum tolerated labelled daily dose, treatment with ACE-I or ARB for at least 4 weeks before visit 1, if not medically contraindicated

排除标准

  • Exclusion criteria is shared in Section 3.2 of the protocol (pages 26-27) there are 17 exclusion criteria

研究者

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