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
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