None listed
Conditions
Interventions
Medical Device : v
Sponsors
Korea Institute of Oriental Medicine
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Males and females aged 19–69 years 2) Those who complained of shoulder area pain after shoulder arthroscopic surgery 3) Those whose visit date is over 2 weeks and under 2 years from the operation date(surgical area fixation is finished). 4) The visual analog scale (VAS) pain score of the surgical area during screening was 40 points or higher. 5) And patients who agreed to sign a written informed consent.
Exclusion criteria
Exclusion criteria: 1) Those who did not submit documents that showed that they had received a shoulder surgery (a surgery certification, a written opinion, a medical certificate, and a medical confirmation) 2) Those to whom application of chimsband intervention was inappropriate due to contact dermatitis or wounds around the lesion 3) Those who utilized narcotic analgesic at the time of screening 4) Those who had suppuration or severe edema of the shoulder’s surgical site and therefore were judged as having acute inflammation or at least one of the test items in the screening exceeded or fell short of 1.5 times or higher of the normal range 5) Participation in other clinical trials 6) Those who had a history of drug or alcohol abuse or was suspected of such abuse 7) And residents of collective dwelling facilities such as social welfare institutions.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Visual Analog Scale (VAS) | — |
Secondary
| Measure | Time frame |
|---|---|
| Shoulder Pain and Disability Index (SPADI);Shoulder Range of Motion (ROM);VAS during sleep;Questionnaire for blood stasis pattern;Number of bands used;Recruitment rate, completion rate, adherence | — |
Countries
Korea, Republic of
Contacts
Public ContactJae Hong Kim
Dongshin University
Outcome results
None listed