EUCTR2018-002822-22-NL进行中(未招募)1 期
S-guided Percutaneous needle tenotomy in Patients with Lateral Elbow Tendinopathy: A multicenter Randomized Controlled Trial - PUNT
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 入组人数
- 114
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
- •Age between 18 and 65 years
- •Pain in the elbow present for more than 12 months, unresponsive to conservative treatment
- •Sonographically proven tendinopathy (hypervascularisation, deep tendon calcifications, hypoechogenic tendon, erosive cortex)
- •Concordant pain during compression with a US Probe in the region of the extensor tendons
- •Is able to give informed consent
- •Is instructable to follow the exercises
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 114
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Surgery related to the lateral elbow tendinopathy, including Needle Aspiration of Calcific Deposits (NACD)
- •Systemic joint disease such as rheumatoid arthritis etc.
- •Rupture or clefts >1cm of the extensor tendons
- •Detachment of extensor tendons or tears in collateral ligament
- •Contraindication for lidocaïne in accordance to the SPC
- •Pregnancy
- •Use of anti-inflammatory drugs, such as NSAIDs, steroids, methotrexate, anti-TNF, azathioprine
- •Use of anticoagulant drugs which is bridged with acetylsalicylate acid
- •Physical, emotional or neurological conditions that would compromise the patient’s compliance with postoperative rehabilitation protocol follow-up (e.g.: drug or alcohol abuse, serious mental illness, or general neurological conditions such as Parkinson, Multiple Sclerosis, etc.)
研究者
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