CTRI/2009/091/000043已完成2 期
Safety and Efficacy of TRC4186 in the treatment of stable heart failure associated with HbA1C â?¥ 6.0% or type 2 Diabetes receiving oral hypoglycaemic therapy (with or without additional insulin) as an add-on to conventional treatment for heart failure.
Torrent Pharmaceutical Ltd0 个研究点目标入组 300 人开始时间: 待定最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 300
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
入选标准
- •Salient Inclusion Criteria
- •Subjects of either sex, aged >= 45 years.
- •Subjects with chronic heart failure, stable for 6 weeks (NYHA class II or III) according to criteria of ESC and on stable medication for heart failure for at least 2 weeks prior to screening.
- •Subjects with Type 2 diabetes mellitus (i.e. receiving oral therapy with or without insulin) or an impaired glucose tolerance (HbA1c should be >= 6.0% at screening).
- •Subjects with an NT-proBNP >= 400 pg/mL (subjects with atrial fibrillation NT-proBNP >= 1200 pg/mL)
- •Subjects receiving at least loop, thiazide or thiazide like diuretic for treating HF
- •Subjects able to undergo cardiopulmonary exercise testing
排除标准
- •Salient Exclusion Criteria
- •CHF caused by myocarditis, cor pulmonale, congenital heart disease, constrictive pericarditis, or hypertrophic or restrictive cardiomyopathy.
- •Acute coronary syndrome or coronary revascularization within 3 months
- •Second-degree or third-degree heart block (unless treated with a pacemaker)
- •Pulmonary function (FEV1) less than 60 % of predicted or requiring long-term corticosteroids.
- •Left ventricular assist device (or an activated minute ventilation pacemaker)
- •Uncontrolled hypertension (systolic blood pressure >= 160 mmHg under antihypertensive treatment).
- •Glomerular filtration rate (eGFR) 30 ml/min.
- •Unwilling or unable to comply with protocol
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