CTRI/2011/09/001987已完成4 期
Comparison of Twice-Daily Insulin Lispro Low Mixture Versus Once-Daily Basal Insulin Glargine and Once-Daily Prandial Insulin Lispro as Insulin Intensification Strategies in Patients With Type 2 Diabetes Who Have Inadequate Glycemic Control on Basal Insulin Glargine and Metformin and/or Pioglitazone
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 478
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
- •Present with type 2 diabetes mellitus
- •-Have been taking metformin and/or pioglitazone
- •-Have received treatment with basal insulin glargine, injected once a day, for greater than or equal to 90 days
- •-Have HbA1c concentration between greater than or equal to 7.5% and less than or equal to 10.5
- •-Have a fasting plasma glucose concentration of less than or equal to 6.7 mmol/L (less than or equal to 121 mg/dL), or greater than 6.7 mmol/L (greater than 121 mg/dL) if the investigator considers that further titration of basal insulin glargine is not possible for safety reasons
- •-Not pregnant or breastfeeding
排除标准
- •-Have Type 1 Diabetes
- •-Their stable dose of pioglitazone is greater than the maximum dose approved for use in combination with insulin in their country
- •-Have a body mass index (BMI) greater than 45 kg/m2.
- •-Have a history of scheduled mealtime (prandial) insulin use within 12 weeks of the screening visit and the total duration of the prandial insulin treatment was greater than 2 weeks
- •-Have had more than one episode of severe hypoglycaemia within 24 weeks prior to entry into the study
- •-Have cardiac disease with a functional status that is Class III or IV
- •-Have a history of renal or liver disease
- •-Have had a blood transfusion or have a blood disorder
研究者
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