IRCT20100718004409N12已完成3 期
The comparison of the effectiveness of high leukocyte PRP, low leukocyte PRP & placebo in treatment of the patients having rotator cuff tendinopathy or partial tear
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 75
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
- 年龄范围
- 40 years 至 no limit（—）
- 性别
- All
入选标准
- •Shoulder pain lasted more than 6 weeks
- •At least 3 positive specific shoulder tests
- •MRI findings implying tendinopathy or partial tear of rotator cuff
排除标准
- •Shoulder pain that lasted less than six weeks
- •The presence of sensory or motor disturbances caused by the cervical radiculer pain
- •Evidence from other pathologies that can lead to shoulder pain. For example, the presence of calcified tendonitis or adhesive capsulitis and ...
- •History of shoulder surgery in the last 6 months
- •The presence of inflammatory rhomatologic diseases such as rheumatoid arthritis, fibromyalgia, poly mialia rheumatica and ...
- •Complete rupture of rotator cuff tendons based on MRI findings
- •The presence of ligamentous laxity or shoulder instability based on physical examination
- •History of corticosteroid, analgesic or hyaluronic acid injection in the shoulder joint over the past 3 months
- •History of exercise therapy and physiotherapy modalities over the past 6 weeks
- •The history of treatment with PRP in the last 6 months
- •Use of other therapies during the intervention period
- •Patients request for discontinuing the treatment
- •Contraindications for performing MRI or PRP in patients
- •Any non-rheumatologic inflammatory disease and severe acute infection in patients
- •Thrombocytopenia in patients
研究者
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