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临床试验/IRCT20161026030511N3
IRCT20161026030511N3已完成3 期

Efficacy and safety endpoints of Ranolazine in comparison with conventional therapy in reduction of HbA1c percentage in type 2 diabetic patients with ischemic heart disease

Samin Daroo Company0 个研究点目标入组 60 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
60

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
50 years 至 no limit(—)
性别
All

入选标准

  • HbA1c more than 6.5%, Age more than 50 year, both genders with diabetes mellitus and coronary artery disease (CAD)
  • Experiencing chronic stable angina for at least 3 months triggered by physical effort and relieved by rest and/or sublingual nitroglycerin
  • CAD documented by one or more of the following: Angiography evidence of more than 50% stenosis of one or more coronary arteries, History of MI, cardiac imaging or exercise test diagnostic for CAD
  • Treatment with up to 2 anti-anginal therapies at a stable dose for at least 2 weeks before starting the trial
  • T2DM patients who use Metformin and Gliclazide

排除标准

  • New York Heart Association class III and IV
  • Acute coronary syndrome in the prior 2 months or planned for coronary revascularization
  • Stroke or transient ischemic attack within 6 months prior
  • QTc more than 500 ms
  • Systolic blood pressure more than 180, diastolic blood pressure more than 110 mmHg
  • Liver cirrhosis
  • Prior treatment with CYP 3A4 inhibitors or P GlyP inductors
  • Treatment with anti arrhythmic medicine class ll and lll
  • Alcohol consumption or drug users
  • Simvastatin consumption

研究者

发起方
Samin Daroo Company

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