NL-OMON20120尚未招募不适用
Effectiveness of Ultrasound Guided Percutaneous treatment of Lateral Epicondylitis using standardized perforation with application of autologous blood, dextrose or perforation only, in relation to pain and functional recovery; A randomized controlled trial
Amphia hospital Breda. OLVG Amsterdam. AMC Amsterdam0 个研究点目标入组 165 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 165
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •Patients referred by their GP to the orthopaedic surgeon diagnosed with unilateral Lateral Epicondylitis lasting longer than 6 weeks
- •Age between 18 and 65 years
排除标准
- •A potential subject who meets any of the following criteria will be excluded from participation in this study:
- •Prior injection therapy (during this episode of LE), surgery or trauma at the affected elbow.
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*Effectiveness of Ultrasound Guided Percutaneous treatment of Lateral Epicondylitis using standardized perforation with application of autologous blood, dextrose or perforation only, in relation to pain and functional recovery; A randomized controlled trial *lateral epicondylitistennis elbow10043237NL-OMON47499Amphia Ziekenhuis165
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