ISRCTN13254422已完成未知
Achilles tendinopathy management (ATM): A multi-centre placebo-controlled randomised trial comparing platelet rich plasma (PRP) to placebo injection in adults with Achilles tendon pain
niversity of Warwick0 个研究点目标入组 240 人开始时间: 2015年10月28日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 240
研究概览
简要总结
2020 Protocol article in https://www.ncbi.nlm.nih.gov/pubmed/32051317 protocol (added 14/02/2020) 2021 Results article in https://pubmed.ncbi.nlm.nih.gov/34255009/ (added 14/07/2021)
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Provision of written informed consent
- •2. Aged 18 years or over
- •3. Pain at the mid-substance of the Achilles tendon for longer than 3 months
- •4. Ultrasound and/or MRI confirmation of tendinopathy
排除标准
- •1. Presence of systemic conditions (including: diabetes, rheumatoid arthritis, peripheral vascular disease)
- •2. Pregnant or actively trying to become pregnant, or breastfeeding at the time of randomisation
- •3. Have had prior Achilles tendon surgery or rupture on the index side
- •4. Previous major tendon or ankle injury or deformity to either lower leg
- •5. Have had a fracture of a long bone in either lower limb in the previous 6 months
- •6. Have any contraindication to receiving a platelet rich plasma injection (haemodynamic instability, platelet dysfunction syndrome, cancer, septicaemia, systemic use of anticoagulant, local infection at site of the procedure)
- •7. Are unable to adhere to trial procedures or complete questionnaires
- •8. Previous randomisation in the present trial
- •Added 19/10/2016:
- •9. Previous PRP treatment into a tendon.
研究者
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