EUCTR2007-001755-19-NL进行中(未招募)不适用
A double-blind Clinical Trial of Benfotiamine Treatment in Diabetic Nephropathy - Benfotiamine in Diabetic Nephropathy
MCG0 个研究点开始时间: 2007年10月26日最近更新:
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •Diabetes mellitus, with onset of disease after the age of 40 years
- •Age: 50-70 years
- •Patients are on treatment with angiotensin converting enzyme inhibitors (ACEi) and/or angiotensin II antagonists (AIIA) in an unchanged dose for at least 3 months
- •Active diabetic nephropathy as indicated by presence of microalbuminuria (30-300 mg/24 h urine) in at least two samples within 2-6 weeks in advance of inclusion in the trial
- •HbA1c < 8.5%, a higher HbA1c ? 9.5% is acceptable if the treating physician and the patient have accepted that striving for lower values is an unreachable goal (patients with high HbA1c values are the ones that one would expect to be benefit most from treatment with benfotiamine)
- •eGFR (estimated by MDRD formula) > 30 ml/min
- •Males and postmenopausal females
- •Written informed consent
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Renal impairment by other causes than diabetes
- •Stage of the disease more severe than indicated in Inclusion criteria
- •(macroalbuminuria or renal insufficiency)
- •Severe hypoglycemia during the last 3 months, needing help from another person
- •Severe hepatopathy (liver function enzymes about three times higher than normal)
- •Endocrine disorders, e.g. hyper-/hypothyroidism
- •Blood pressure > 160/90 mmHg
- •Severe cardiac function disturbances and severe heart rhythm disturbances
- •Severe general diseases or mental disorders making the participation in the study
- •Drug abuse
- •Female patients during pregnancy and lactation period and female patients with active menses during the past year
- •Hypersensitivity to benfotiamine or other constituents of the study medication
- •HbA1c >9.5%
- •Use of vitamin B containing supplements during the last 3 months
- •Use of NSAIDs more than 3x per week (including self-medication)
- •Participation in another study within one month before joining the benfotiamine
研究者
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