None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Male or female aged over 18. 2) Patients suffering from shoulder pain and diagnosed with one of the following disease classficiation codes: M2531, M2551, M6261, M750-759, M7911, M79110, M7981, M7991, S400, S434, S437, S44, S46, S49 3) Patients who can communicate sufficiently with the researcher and write the questionnaire 4) Patients who has voluntarily agreed to participate and written informed consent form
Exclusion criteria
Exclusion criteria: 1) Patients diagnosed with inflammatory joint disease or neoplastic disorder and taking drugs related to these diseases. 2) Referred pain from spinal disease related to cervical spine 3) Mental illness that can not follow clinical test compliance 4) Musculoskeletal disorders that may affect the efficacy assessment, or any joint disease that is considered impossible to participate in this observational study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 100mm pain VAS (visual analogue scale) | — |
Secondary
| Measure | Time frame |
|---|---|
| Shoulder Pain and Disability Index (SPADI) ;Shoulder range of motion (ROM) ;EuroQol-5 dimensions-5 Levels (EQ-5D-5L) ;Treatment satisfaction evaluation;Safety - Adverse event | — |
Countries
Korea, Republic of
Contacts
Kyung Hee University Oriental Medicine Hospital at Gangdong