CTRI/2010/091/001280已完成4 期
A multicentre, open label, observational, non-interventional study to evaluate the safety and effectiveness of liraglutide in subjects with type 2 diabetes mellitus in India
ovo Nordisk India Private Ltd0 个研究点目标入组 1,386 人开始时间: 待定最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 1,386
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Pms
入排标准
入选标准
- •Subjects with Type 2 Diabetes, including newly-diagnosed patients / those already receiving other anti-diabetic medications including GLP-1 analogues, who require treatment with liraglutide according to the clinical judgment of their treating physician
- •Subjects who are capable of giving study-specific signed informed consent before any collection of information
- •Age 18 years and older
排除标准
- •Subjects with type 1 diabetes
- •Subjects who are or have previously been on liraglutide
- •Subjects who have previously been enrolled in the study
- •Subjects who are participating in another clinical trial
- •Subjects with a hypersensitivity to liraglutide or to any of the excipients (Disodium phosphate dihydrate, propylene glycol, phenol, water for injections)
- •Subjects who are pregnant, breast feeding or have the intention of becoming pregnant within the following 6 months
研究者
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