A prospective, controlled, randomized, double blind, comparative, parallel,2-arm study to evaluate the efficacy and safety of Epalrestat (150 mg) compared to Methylcobalamine (1500 Âµg) in patients suffering from diabetic peripheral neuropathy

Primary Investigator0 个研究点目标入组 100 人开始时间: 待定最近更新: 2021年11月24日

试验速览

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•1. Patients of either sex in the age group between 20 to 70 years.
•2. Diabetic patients stabilized on antidiabetic medication (on stable dose of antidiabetic drugs for the last 4 weeks) with stable glycemic control (HbA1c < 9%, with Â± 0.5% variation in the previous 3 months) presenting with subjective symptoms of peripheral neuropathy confirmed on the basis Modified neuropathy disability score >2.
•3. Subjects who provide a written informed consent to abide by the study requirements.

•1. Patients with stage 3(N3)19i.e.disabling neuropathy or presence of symptoms/
•Signs of foot ulcer.
•2. Patients with diabetic neuropathy requiring hospital admission for management of neuropathy/ diabetic complications / any other disease conditions.
•3. Patients presenting with primary cause of neurologic disorders other than diabetes (alcoholic neuropathy, carpal tunnel syndrome, sequelae of cerebrovascular disease).
•4. Patients presenting with arteriosclerosis obliterans (ankle brachial pressure index of < 0.8)
•5. Patients with known hypersensitivity to any of the ingredients of the test /
•comparator formulation.
•6. Patients with severe cardiac, hepatic, gastrointestinal, renal, pulmonary and skin diseases.
•7. Patients with H/O alcohol/ drug abuse
•8. Pregnant and lactating females.
•9. Simultaneous participation in another clinical study or if they were receiving other experimental medications for diabetic neuropathy, prostaglandin E1 preparations, or any other medication that affects symptoms of diabetic neuropathy.

发起方

Primary Investigator