ISRCTN12951626已完成不适用
A pilot study of platelet-rich plasma (PRP) versus autologous whole blood versus saline in the treatment of resistant tennis elbow
The Robert Jones and Agnes Hunt Orthopaedic Hospital NHS Foundation Trust0 个研究点目标入组 30 人开始时间: 2015年7月16日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 30
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
- 性别
- All
入选标准
- •1. Established lateral epicondyle tendinopathy with a minimum symptom duration of 3 months
- •2. Aged 18 or above and below 65
- •3. Willing to avoid the use of topical and oral nonsteroidal anti-inflammatory drugs for a period of 6 weeks following injection
- •4. Has completed the study physiotherapy program for a minimum period of 6 weeks with no improvement in symptoms
- •Target Gender: Male & Female; Upper Age Limit 65 years ; Lower Age Limit 18 years
排除标准
- •1. Bilateral tennis elbow
- •2. Currently taking part in any interventional study that may impact upon study outcomes.
- •3. A concomitant injury that may impact on the ability to complete outcome assessments
- •4. Previous surgical intervention of the tendinopathy
- •5. Inflammatory disease, or chronic widespread pain syndrome
- •6. Requires regular use of anti-inflammatory medication for complaints other than Tennis Elbow
- •7. Known platelet dysfunction or thrombocytopaenia, or haemodynamic instability
- •8. Malignancy
- •9. Unable or unwilling to complete the 12 month follow-up assessments
- •10. Unable to communicate fluently in English or an inability to respond to validated questionnaires written in the English language
- •11. Platelet count <105/microlitre
- •12. Corticosteroid injection at the treatment site within the last 4 weeks, or systemic use of corticosteroids within the last 2 weeks. Anti-coagulation therapy within 5 days before treatment
- •13. Treatment with Non-steroidal anti-inflammatory drugs within 1 week prior to treatment
- •14. Septicaemia or fever
研究者
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