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临床试验/IRCT20230501058035N2
IRCT20230501058035N2招募中2 期

Comparison of the effect of oral empagliflozin and placebo on cardiovascular function and quality of life in patients with acute myocardial infarction: a randomized, double-blind clinical trial.

Hamedan University of Medical Sciences0 个研究点目标入组 354 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
招募中
入组人数
354

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 80 years(—)
性别
All

入选标准

  • Diagnosis of ST elevation MI acute myocardial infarction by a cardiologist based on clinical variables and ECG
  • Glomerular filtration rate (rGFR) more than 30
  • Systolic blood pressure before the first dose of the drug more than 110
  • Diastolic blood pressure before the first dose of medicine more than 70
  • The first dose of drug administration less than 72 hours after the occurrence of an acute stroke

排除标准

  • People with diabetes other than type 2
  • History of diabetic ketoacidosis
  • Hemodynamic instability caused by intravenous administration of catecholamine, calcium sensitizers, or phosphodiesterase inhibitors
  • Acute symptomatic urinary tract infection
  • Genital infection
  • Continuous treatment with SGLT2 inhibitors
  • Being treated with any SGLT-2 inhibitor (dapagliflozin, canagliflozin, empagliflozin) four weeks before the screening visit.
  • Known allergy to SGLT-2 inhibitors
  • Severe hypoglycemia in the last six months treated with insulin or sulfonylurea
  • Symptomatic acute urinary tract infection (UTI) or genital infection
  • Patients currently receiving treatment with any SGLT-2 inhibitor (dapagliflozin, canagliflozin, empagliflozin).

研究者

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