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临床试验/NCT01536652
NCT01536652已完成不适用

Prandial Oriented NovoMix 30® - the Physiological Insulin Therapy of Diabetes Type 2

Novo Nordisk A/S0 个研究点目标入组 4,994 人开始时间: 2006年1月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
4,994
主要终点
HbA1c (glycosylated haemoglobin)

研究概览

简要总结

This study is conducted in Europe. The aim of this observational study is to document the glycaemic parameters, adverse events, including drug reactions, as well as hypoglycaemic episodes, in patients that switched from insulin glargine combined with oral antidiabetic drugs (OADs) to biphasic insulin aspart 30 (NovoMix® 30) combined with OADs, when applicable.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Subjects with diabetes mellitus type 2

排除标准

  • 未提供

研究组 & 干预措施

BIAsp 30 users

干预措施: biphasic insulin aspart 30 (Drug)

结局指标

主要结局

HbA1c (glycosylated haemoglobin)

次要结局

  • Insulin dosage
  • Incidence of (serious) adverse drug reactions
  • Incidence of hypoglycaemic episodes
  • Body weight
  • Preprandial and postprandial blood glucose values (self measured)

研究者

申办方类型
Industry
责任方
Sponsor

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