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临床试验/NCT00393718
NCT00393718已完成3 期

Effect of Liraglutide on Glycaemic Control in Subjects With Type 2 Diabetes

Novo Nordisk A/S1 个研究点 分布在 1 个国家目标入组 400 人开始时间: 2006年11月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
400
试验地点
1
主要终点
Glycosylated Haemoglobin A1c (HbA1c) After 24 Weeks of Treatment

研究概览

简要总结

This trial is conducted in Japan. The trial aims for comparison of the effect on glycaemic control of liraglutide, compared to sulfonylurea (SU treatment), as assessed by HbA1c after 24 and 52 weeks in subjects with type 2 diabetes. Trial has a randomisation period of 24 weeks followed by a 28 week extension period, in total 52 weeks.

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
Double (Participant, Investigator)

入排标准

年龄范围
20 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Type 2 diabetes
  • Diet/exercise therapy with or without an oral anti-diabetic drug for at least eight weeks
  • HbA1c greater than or equal to 7.0% and less than 10.0%
  • BMI (Body Mass Index) less than 35 kg/m2

排除标准

  • Treatment with insulin within the last 12 weeks
  • Treatment with any drug that could interfere with the glucose level
  • Any serious medical condition
  • Females who are pregnant, have intention of becoming pregnant or are breastfeeding

研究组 & 干预措施

Glibenclamide

Active Comparator

Glibenclamide 1.25-2.5 mg + liraglutide placebo

干预措施: placebo (Drug)

Liraglutide

Experimental

Liraglutide 0.9 mg + glibenclamide placebo

干预措施: liraglutide (Drug)

Liraglutide

Experimental

Liraglutide 0.9 mg + glibenclamide placebo

干预措施: placebo (Drug)

Glibenclamide

Active Comparator

Glibenclamide 1.25-2.5 mg + liraglutide placebo

干预措施: glibenclamide (Drug)

结局指标

主要结局

Glycosylated Haemoglobin A1c (HbA1c) After 24 Weeks of Treatment

时间窗: after 24 weeks of treatment

次要结局

  • Glycosylated Haemoglobin A1c (HbA1c) After 52 Weeks of Treatment(after 52 weeks of treatment)
  • Fasting Plasma Glucose After 24 Weeks of Treatment(after 24 weeks of treatment)
  • Fasting Plasma Glucose After 52 Weeks of Treatment(after 52 weeks of treatment)
  • Postprandial Glucose AUC After 24 Weeks of Treatment(after 24 weeks of treatment)
  • Postprandial Glucose AUC After 52 Weeks of Treatment(after 52 weeks of treatment)
  • Mean PG in 7-point Plasma Glucose Profile After 24 Weeks of Treatment(after 24 weeks of treatment)
  • Mean PG in 7-point Plasma Glucose Profile After 52 Weeks of Treatment(after 52 weeks of treatment)
  • Mean Postprandial PG Increment in 7-point Plasma Glucose Profile After 24 Weeks of Treatment(after 24 weeks of treatment)
  • Mean Postprandial PG Increment in 7-point Plasma Glucose Profile After 52 Weeks of Treatment(after 52 weeks of treatment)
  • Body Weight After 24 Weeks of Treatment(after 24 weeks of treatment)
  • Body Weight After 52 Weeks of Treatment(after 52 weeks of treatment)
  • Hypoglycaemic Episodes(over 52 weeks of treatment)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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