KCT0002751招募中未知
Effectiveness and safety of fluoroscopy-guided acupuncture for subacromial impingement syndrome; a randomized, patient-assessor blind, parallel clinical trial
Wonkwang University, Gwangju Medical Center0 个研究点目标入组 54 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 发起方
- 入组人数
- 54
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional Study
入排标准
- 年龄范围
- 25(Year) 至 65(Year)（—）
- 性别
- All
入选标准
- •1) Males and females aged 25 to 65 years old, with no limitation of shouler motion of range
- •2) Those who have the shoulder pain lasting more than 2 months from the onset and the pain is worse when sleeping sideways or lifting the arm over the head, with positive on Neer or Hawkins test, with more than 50 mm on pain of visual analogue scale(VAS), who can be diagnosed as subacromial impingement syndrome by excluding fracture, dislocation, degenerative arthropathy, os acromiale, subacromial spur, and calcific tendinitis in plain radiography.
- •3) Those who have minimal help with the nature of the pain and are able to communicate sufficiently with the researcher and write a questionnaire.
- •4) Those who have pledged not to receive treatment other than the prescribed treatment within the period of study.
- •5) Agreed with written informed consent voluntarily.
排除标准
- •1) History of shoulder surgery, fracture, dislocation trauma
- •2) Patients with disorders of the cervical spine or other upper extremity that has a significant impact on the shoulder
- •3) Patients who received injection treatment on shoulder within 6 months
- •4) Patients with fracture, dislocation, degenerative arthropathy(GH joint, AC joint) os acromiale, subacromial spur ,and calcific tendinitis of the shoulder in plain radiography
- •5) Patients with positive findings in physical examination(drop arm test, empty can test) for exclusion of rotator cuff tear
- •6) Patients with positive findings in physical examination(Yergason test) for exclusion of biceps tendinitis
- •7) Patients who diagnosed as a frozen shoulder (adhesive capsulitis) in range of motion test
- •8) Patients with clinically meaningful medical conditions (pacemaker insertion, significant arrhythmia on electrocardiography, etc.) under the judgment of the researcher
- •9) Patients with concomitant disorders contraindicated to Acetaminophen or hypersensitivity to Acetaminophen(Acetaminophen is relief medication in this study)
- •9) Pregnant or breastfeeding female patients, patients with positive findings in the urine pregnancy test before random assignment, patients who are unable or unwilling to use appropriate contraceptive methods (hormonal contraceptives, condoms, intrauterine devices, etc.) to avoid pregnancy throughout the entire trial period
- •10) Patients with mental disorders who can not follow the this clinical trial protocol
- •11) Patients who were considered as unsuitable for participation by the researcher
研究者
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