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临床试验/ACTRN12607000492459
ACTRN12607000492459已完成不适用

A randomised placebo-controlled trial to determine the effectiveness of pulsed electrical stimulation (E-PES) in the management of osteoarthritis of the knee as measured by changes in pain, function and patient global assessment.

Robyn Fary0 个研究点目标入组 70 人开始时间: 2007年9月24日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
70

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 -2147483648 No limit(—)
性别
All

入选标准

  • Primary knee osteoarthritis diagnosed using the American College of Rheumatology modified clinical classification criteria; persistent, stable pain for a minimum of three months; pain score of at least 25mm on a 100mm visual analogue scale

排除标准

  • Co-existing inflammatory arthropathies, contraindications to electrical stimulation, existence of skin disorders in the area of the knee to be treated, scheduled to have a knee joint replacement during the study period, unable to read or understand English

研究者

发起方
Robyn Fary

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