CTRI/2010/091/000223已完成3 期
A phase 3, single blind, randomized, comparative, multicentric clinical study to evaluate efficacy and safety of FDC of Epalrestat 50 mg + Methylcobalamin 500 mcg with Epalrestat 50 mg in the treatment of patients with Diabetic neuropathy.
Aristo Pharmaceuticals pvt. ltd.0 个研究点目标入组 220 人开始时间: 待定最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 220
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
- •Age > 18 yrs, Type 2 diabetes treated with oral hypoglycemics with evidences of neuropathy, informed consent
排除标准
- •no or low score for diabetic neuropathy, other type of neuropathy, other medications, patients with peripheral vascular diseases.
研究者
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