EUCTR2012-000866-40-IT进行中（未招募）不适用
Evaluation of the efficacy and suppression of the hypothalamic-pituitary-adrenal axis resulting in intrabursale single administration of cortisone in patients with calcific tendonitis of the rotator cuff '': randomized, controlled clinical trial - TPESP 2011-12
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •Patients of both sexes, aged between 30-50 years, suffering from painful calcific tendonitis of the shoulder (calcification or mature phase of resorption) confirmed by ultrasound examination.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range: 0
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 40
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •enthesitis calcific shoulder
- •calcific tendinopathy with lesions of the rotator cuff
- •Septic arthritis or infection of the superficial tissues or periarticular
- •Disease hematologic or coagulation (liver failure ....)
- •metabolic diseases (diabetes)
- •Organ Transplant
- •collagenopatiche diseases or systemic inflammatory rheumatic (SLE, RA ..)
- •previous use of cortisone 2 months prior to TPE
- •Concomitant therapy with anticoagulants and / or antiplatelet
- •A history of asthma, allergic rhinitis, allergic conjunctivitis, bronchiectasis, sarcoidosis (erythema nodosum, uveitis ..), cystic fibrosis, COPD, Crohn's, ulcerative colitis
- •are allergic to cortisone derivatives
- •Pregnant or lactating
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