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临床试验/NCT01585506
NCT01585506已完成不适用

Psychosocial Factors Related to Compliance With Treatment With Biphasic Insulin Analogues

Novo Nordisk A/S1 个研究点 分布在 1 个国家目标入组 3,618 人开始时间: 2010年9月20日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
3,618
试验地点
1
主要终点
Frequency and level of difficulty in introducing changes in compliance with the guidelines for biphasic insulin analogue use in subjects previously treated with biphasic human insulins

研究概览

简要总结

This study is conducted in Europe. The aim of this study is to investigate psychosocial factors related to compliance with treatment with biphasic insulin analogues.

研究设计

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

入排标准

性别
All
接受健康志愿者

入选标准

  • Patients with type 2 diabetes in whom therapy with biphasic insulin analogues was started

排除标准

  • 未提供

结局指标

主要结局

Frequency and level of difficulty in introducing changes in compliance with the guidelines for biphasic insulin analogue use in subjects previously treated with biphasic human insulins

时间窗: Up to 3 months

次要结局

  • Correlations between the difficulty in introducing changes in compliance with the guidelines for biphasic insulin analogue use in subjects previously treated with biphasic human insulins, and psychosocial factors(Up to 3 months)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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