None listed
Conditions
Interventions
Medical Device : 1. Clinical trial device : CGM MB-1401
2. Management : Subjects performed the following 20 treatments according to the randomly assigned group.
- Experimental group : CGM MB-1401,
Sponsors
Presbyterian Medical Center
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Adult men and women with muscle pain on neck, upper back, and lower back 2) Subjects who are determined to be suitable in the screening test 3) Subjects who have received a detailed explanation of the study and completed consent form.
Exclusion criteria
Exclusion criteria: 1) Patients with muscle pain due to diseases of other organs such as liver disease, cancer, rheumatic diseases, thyroid diseases, etc. 2) myopathy 3) Malignant tumor, spinal cord infection, or thrombosis 4) Skin disease and hypersensitivity 5) Spinal deformity or neurological abnormalities - Above 20 degrees of Cobb’s angle in Scoliosis - History of spinal fractures due to severe osteoporosis 6) Fail Back Syndrome after Spinal surgery 7) Risk of vertebral fractures 8) Reduced skin sensation 9) Those who have received other investigational drugs or are applying the investigational medical device 30 days before the start of the clinical trial 10) A person deemed inappropriate as a clinical trial subject when judged by the investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Surface EMG | — |
Secondary
| Measure | Time frame |
|---|---|
| Pain Disability Index;Digital Pain Scale;Thermography;Ultrasonography;MULTIDIMENSIONAL FATIGUE INVENTORY - 20;Korean Occupational Stress Scale;Stress Response Inventory;Inbody;Sympathetic Skin Reponse;Beck Depression Inventory | — |
Countries
Korea, Republic of
Contacts
Public ContactJi Sun Oh
Presbyterian Medical Center
Outcome results
None listed