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临床试验/NCT01200745
NCT01200745Unknown不适用

Efficacy of Topical Capsaicin on Chronic Neck Pain ; Double-blinded Randomized Trial

Kyunghee University Medical Center1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2010年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
入组人数
60
试验地点
1
主要终点
Pain Scores on the Visual Analogue Scale(VAS)

研究概览

简要总结

The purpose of this study is to determine whether topical capsaicin patch can effectively reduce chronic neck pain.

详细描述

  • Design: This is a double-blind, randomized, controlled study. Participants: Sixty participants with chronic neck pain are recruited and randomly assigned to two groups.
  • Intervention: Over an four-week period, the treatment group (n=30) uses capsaicin patch (100 mcg/3cc) at the tender point of neck for 12 hours a day; the control group (n=30) receives Hydrogel patch instead of capsaicin patch.

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
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Korean participants with Chronic neck pain are enrolled in our study

排除标准

  • Participants with coagulation deficiencies, infections, hypertension, diabetes, heart disease, renal disease, liver disease, cancer, myelopathy, hypersensitivity of drugs, other skeletomuscular disease, allergic response to capsaicin, pregnancy and nursing are excluded

研究组 & 干预措施

capsaicin patch

Active Comparator

干预措施: Capsaicin patch (Drug)

Hydrogel patch

Placebo Comparator

干预措施: Capsaicin patch (Drug)

结局指标

主要结局

Pain Scores on the Visual Analogue Scale(VAS)

时间窗: 4 week

次要结局

  • Neck disability index(4 week)
  • Beck depression inventory(4 week)
  • SF-36(4 week)
  • EQ-5D(EuroQol-5 dimension)(4 week)

研究者

申办方类型
Other

研究点 (1)

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