The primary objective of this study is to prospectively determine, at 10 days after orthopedic shoulder or knee surgery, if pulsed electromagnetic field (PEMF) therapy is beneficial in reducing patient-reported post-operative pain, as measured by visual analog scale (VAS). The amount of pain medication taken daily and the physical function outcome scores after surgery and PEMF treatment will also be measured.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
76
The active device emits PEMF signal whereas the placebo device does not emit a PEMF signal. The active device is on for 15 minutes at a time, every two hours, for 10 days.
Stanford University
Redwood City, California, United States
RECRUITINGMean change from baseline in pain scores on the visual analog scale (VAS) at 10 days
The VAS is a subjective pain scale from 0 to 10, with 0 representing no pain.
Time frame: 10 days
Mean change from baseline in narcotic pain medicine use at 10 days
Pain medication will be documented every 24 hours.
Time frame: 10 days
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