KCT0002751
Recruiting
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 sites54 target enrollmentTBD
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Wonkwang University, Gwangju Medical Center
- Enrollment
- 54
- Status
- Recruiting
- Last Updated
- 7 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •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.
Exclusion Criteria
- •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
Outcomes
Primary Outcomes
Not specified
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