The purpose of this study is to determine whether use of the nCap Medical Nano-Capacitive pain relief patch reduces subject pain as measured by subject pain scores, WOMAC scores (pain, stiffness and physical function), global assessment scores, and pain medication change as compared to participants randomly assigned to the sham patch group.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
70
Each participant will be randomly assigned to sham or actual patch. Patches will be worn for 3 weeks. Pain and quality of life will be assessed and compared between groups
Sham patch will be worn for 3 weeks exactly like actual pain patch
Knee Arthritis Clinical Trial Officew
Salt Lake City, Utah, United States
RECRUITINGPain score using VAS scale
0-10 pain scale
Time frame: After 30 minutes of use
WOMAC score
arthritis assessment score
Time frame: 3 weeks
Sustained pain response
0-10 VAS pain score
Time frame: 3 weeks
Global assessment question
How the patient feels they are doing
Time frame: 3 weeks
Pain medication monitoring
Tylenol use
Time frame: 3 weeks
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