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临床试验/NCT00476151
NCT00476151已完成2 期

A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study of the Efficacy and Safety of EpiCept™ NP-1 Topical Cream in Patients With Pain From Diabetic Peripheral Neuropathy (DPN)

EpiCept Corporation1 个研究点 分布在 1 个国家目标入组 226 人开始时间: 2007年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
226
试验地点
1
主要终点
Placebo vs. Active Comparison of the Change From Average Pain at Baseline to Average Pain at 4 Weeks.

研究概览

简要总结

This is a multicenter, randomized, placebo-controlled, parallel group study of EpiCept™ NP-1 Topical Cream (amitriptyline 4%/ketamine 2%) in approximately 200 patients with pain in the lower extremities due to diabetic nerve pain.

详细描述

This is a phase II, multicenter, randomized, placebo-controlled, parallel group study of EpiCept™ NP-1 Topical Cream (amitriptyline 4%/ketamine 2%) in approximately 200 patients with chronic pain in the lower extremities due to diabetic peripheral neuropathy (DPN).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult patients with chronic pain due to diabetic peripheral neuropathy (DPN) of at least 6 months duration are eligible if they have an average daily pain score of > 4 during the baseline week.

排除标准

  • Clinically significant intercurrent illness (e.g., endocrine, cardiac, hepatic, renal, neurologic, hematologic, skeletal) that the investigator determines could interfere with the efficacy or safety assessments in this study

研究组 & 干预措施

placebo cream

Placebo Comparator

vehicle cream

干预措施: placebo cream (Drug)

amitriptyline 4% ketamine 2% cream

Active Comparator

active topical cream

干预措施: EpiCept NP-1 (4% Amitriptyline/ 2% Ketamine) Topical Cream (Drug)

结局指标

主要结局

Placebo vs. Active Comparison of the Change From Average Pain at Baseline to Average Pain at 4 Weeks.

时间窗: baseline and 4 weeks treatment

diabetic peripheral neuropathy (DPN) pain is recorded on a numerical rating scale of 0 (no pain) to 10 (worst possible pain) at baseline and the endpoint of 4 weeks.

次要结局

未报告次要终点

研究者

发起方
EpiCept Corporation
申办方类型
Industry

研究点 (1)

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