The Comparison O the Efficacy of Mesotherapy and Intra-articular Steroid Injection in Patients with Chronic Shoulder Pain
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 84
- 试验地点
- 2
- 主要终点
- VAS (Visual Analouge Scale)
研究概览
简要总结
Patients with chronic shoulder pain will be divided randomly into mesotherapy and intra-articular steroid injection groups. Pain severity, range of motion and functional impairment will evaluated before treatment, 30 minutes and 4 weeks after the injections.
详细描述
The study will include 84 patients aged 18-75 who applied to physical medicine and rehabilitation out-patient clinic with chronic shoulder pain between May and July 2024. Patients will be randomly divided into two groups: a mesotherapy group and steroid injection group, using the closed-envelope method. In the first group, a total of 3 sessions of mesotherapy are applied to the shoulder areas of the patients, 7 days apart. A single-session intra-articular 20 mg triamcinolone hexacetonide injection will be administered for patients in group 2. Pain severity, range of motion and functional impairment will evaluated before treatment, 30 minutes and 4 weeks after the injections.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Single (Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 75 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Having shoulder pain for 6 months
- •VAS (Visual Analog Scale) > 4
- •Patients who can receive verbal instructions and do not have cognitive deficits
排除标准
- •Physical therapy applied to the shoulder area in the last 3 months
- •Having had a shoulder joint injection in the last 3 months
- •History of previous upper extremity surgery
- •History of drug allergy
- •Use of anticoagulant drugs (warfarin, low molecular weight heparin), patients with coagulation disorder
- •History of malignancy
- •Psychiatric illness
- •A rheumatological diagnosis such as Polymyalgia Rheumatica, Rheumatoid Arthritis, Ankylosing Spondylitis
- •Kidney failure
- •Liver disease
- •Heart failure
- •Presence of infection, wound, allergy, burn-like lesions in the application area
结局指标
主要结局
VAS (Visual Analouge Scale)
时间窗: Patients will be evaluated before treatment, 30 minutes and 4 weeks after the injections.
Pain Severity evaluation ((0 (no pain)-10 (unbearable pain))
Shoulder Disability Questionnaire' (OSS) form
时间窗: Patients will be evaluated before treatment, 30 minutes and 4 weeks after the injections.
Functional Disability evaluation (0-100)
Goniometric shoulder range of motion
时间窗: Patients will be evaluated before treatment, 30 minutes and 4 weeks after the injections.
shoulder range of motion evaluation
次要结局
未报告次要终点
研究者
Ecem Pelin Kaymaz
Medical Doctor of Physical Medicine and Rehabilitation
Haydarpasa Numune Training and Research Hospital