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临床试验/NCT01680263
NCT01680263已完成不适用

Kinesiotaping in Treatment of Pes Anserinus Tendino-bursitis

Shiraz University of Medical Sciences1 个研究点 分布在 1 个国家目标入组 46 人开始时间: 2012年2月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
46
试验地点
1
主要终点
Pain (VAS)and swelling scores

研究概览

简要总结

The aim of this study was to determine the effects of kinesiotaping in comparison to NSAIDs and physical therapy in treatment of pes anserinus tendino-bursitis.

详细描述

The treatment of pes anserinus tendino-bursitis includes refraining from aggravating activities, local modalities such as heat, ice, ultrasound (US), iontophoresis, phonophoresis, electrical stimulation (ES), nonsteroidal anti-inflammatory drugs (NSAIDs) and injections with either corticosteroids or local anesthetics. Another treatment that seems to have a significant effect on the improvement of the disease is kinesiotaping. Kinesiotaping is a cotton strip with an acrylic adhesive that is used for treating athletic injuries and a variety of physical conditions. The therapeutic effects of the tape is to relax the overused muscles and in rehabilitation to facilitate the underused muscles. Advocates claim that the wave pattern found on the kinesiotaping has a lifting effect on the skin which can diminish swelling and inflammation via improving circulation and reduce pain by removing pressure from pain receptors.

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
Single (Outcomes Assessor)

入排标准

年龄范围
20 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with clinical diagnosis of pes anserinus tendino-bursitis.

排除标准

  • Previous history of trauma or surgery on the knee joint,
  • History of NSAIDs induced acid-peptic disease
  • Systemic and rheumatic diseases

研究组 & 干预措施

Kinesiotaping

Experimental

Use of kinesiotaping on the painful area in the form of "space correction". Kinesiotaping was repeated for 3 weeks with 1 week interval

干预措施: Kinesiotaping (Device)

NSAIDs/Physical therapy

Active Comparator

treatment was done with NSAIDs and 10 sessions of daily physical therapy.

干预措施: NSAIDs/Physical therapy (Procedure)

结局指标

主要结局

Pain (VAS)and swelling scores

时间窗: 3 weeks

Visual analog scale for pain evaluation Assessment of the local swelling via palpation

次要结局

  • The number of participants with adverse events(3 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Kaynoosh Homayouni

Assistant professor of Physical Medicine and Rehabilitation

Shiraz University of Medical Sciences

研究点 (1)

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