NCT01165684已完成4 期
A Randomised, Controlled, Open Label, Multicentre, Multinational, Treat-to-target Trial Investigating the Efficacy and Safety of Intensification With Addition of Bolus Insulin Aspart in Subjects With Type 2 Diabetes Inadequately Controlled on Basal Insulin With or Without Oral Anti-diabetic Drugs: Step-wise Addition Versus Complete Basal-bolus Therapy
适应症
干预措施
相关药物
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 401
- 试验地点
- 1
- 主要终点
- Change in Glycosylated Haemoglobin (HbA1c) From Baseline to Week 32
研究概览
简要总结
This trial is conducted in Europe, and North and South America. The aim of this clinical trial is to investigate if the two treatments are equally effective.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Type 2 diabetes (diagnosed clinically) for at least 12 months
- •Basal insulin treatment (NPH once or twice daily, insulin glargine once daily or insulin detemir once daily) for at least 6 months
- •HbA1c: 7.0-9.0 % (both inclusive) by central laboratory analysis (one retest analysed at the central laboratory within a week is permitted with the result of the last sample being conclusive)
- •BMI (Body Mass Index) less than 40.0 kg/m^2
排除标准
- •Previous use of pre-mix or bolus insulin (allowed is previous use of bolus insulin only in case of a hospitalisation or a severe condition requiring intermittent use of bolus insulin for less than 14 consecutive days, but not during the last 6 months prior to screening visit (Visit 1)
- •Use of GLP-1 (Glucagon-like peptide-1) receptor agonists or pramlintide within the last 6 months prior to prior to screening visit (Visit 1)
- •Anticipated change in concomitant medication known to interfere significantly with glucose metabolism (e.g. systemic corticosteroids, beta-blockers, MAO (Monoamine oxidase) inhibitors, etc.)
- •Cardiovascular disease, within the last 12 months prior to screening visit (Visit 1), defined as: stroke; decompensated heart failure New York Heart Association (NYHA) class III or IV; myocardial infarction; unstable angina pectoris; or coronary arterial bypass graft or angioplasty
- •Uncontrolled treated/untreated severe hypertension (systolic blood pressure sitting at least 180 millimetre (mm) mercury (Hg) and/or diastolic blood pressure at least 100 mmHg). For Argentina: systolic blood pressure sitting at least 150 mmHg and/or diastolic blood pressure at least 90 mmHg
- •Impaired liver function, defined as ALAT (Alanine aminotransferase) at least 2.5 times upper limit of normal (one retest analysed at the central laboratory within a week is permitted with the result of the last sample being conclusive)
- •Impaired renal function defined as serum creatinine above 135 micromol/L (above 1.5 mg/dL) for males and above 110 micromol/L (above 1.2 mg/dL) for females; and, if required by the locally applicable metformin label, glomerular filtration rate below 60 ml/min, calculated by the Cockroft & Gault formula). One retest within a week is permitted with the result of the last sample being conclusive
- •Recurrent severe hypoglycaemia (more than 1 severe hypoglycaemic episode, during the last 12 months) or hypoglycaemic unawareness as judged by the Investigator or hospitalisation for diabetic ketoacidosis during the previous 6 months
- •Proliferative retinopathy or maculopathy requiring treatment according to the Investigator
- •Treatment with OADs (Oral anti-diabetic drug) contraindicated or unapproved for combination treatment with insulin (according to local OAD label)
研究组 & 干预措施
Step-wise
Experimental
干预措施: insulin aspart (Drug)
Step-wise
Experimental
干预措施: insulin detemir (Drug)
Basal-bolus
Active Comparator
干预措施: insulin aspart (Drug)
Basal-bolus
Active Comparator
干预措施: insulin detemir (Drug)
结局指标
主要结局
Change in Glycosylated Haemoglobin (HbA1c) From Baseline to Week 32
时间窗: Week 0, Week 32
Estimated mean change from baseline in HbA1c after 32 Weeks of treatment
次要结局
- Fasting Plasma Glucose (FPG) at Week 21(Week 21)
- Body Mass Index (BMI) at Week 32(Week 32)
- Change in Glycosylated Haemoglobin (HbA1c) From Baseline to Week 10(Week 0, Week 10)
- Mean Plasma Glucose Increment Over 3 Meals (Breakfast, Lunch and Dinner) at Week 32(Week 32)
- Body Weight at Week 32(Week 32)
- Proportion of Subjects Reaching Glycosylated Haemoglobin (HbA1c) Below 7.0% at Week 10(Week 10)
- Proportion of Subjects Reaching Glycosylated Haemoglobin (HbA1c) Below 7.0% at Week 21(Week 21)
- Fasting Plasma Glucose (FPG) at Week 10(Week 10)
- Mean Plasma Glucose Increment Over 3 Meals (Breakfast, Lunch and Dinner) at Week 10(Week 10)
- Mean Plasma Glucose Increment Over 3 Meals (Breakfast, Lunch and Dinner) at Week 21(Week 21)
- Change in Glycosylated Haemoglobin (HbA1c) From Baseline to Week 21(Week 0, Week 21)
- Hypoglycaemic Episodes (Rate of All Treatment Emergent Hypoglycaemia Episodes)(Week 0 to Week 32)
- Proportion of Subjects Reaching Glycosylated Haemoglobin (HbA1c) Below 7.0% at Week 32(Week 32)
- Fasting Plasma Glucose (FPG) at Week 32(Week 32)
研究者
研究点 (1)
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