A prospective cohort follow-up study design is undertaken. Both males and females with mild to moderate carpal tunnel syndrome will receive standard-of-care wrist splint for 6 weeks and undergo follow up studies for data collection. Controls will also be seen for a one time visit.
Study Type
OBSERVATIONAL
Enrollment
213
UC Davis Medical Center
Sacramento, California, United States
Cross sectional area of median nerve using ultrasound
Time frame: 6 weeks
Patient-reported outcome measures using NeuroQOL and CTSAQ
Time frame: 6 weeks
Motor latency, motor amplitude, sensory velocity and sensory amplitude with electrodiagnostic study
Time frame: 6 weeks
cross sectional area, electrodiagnostic study, age, gender, height, weight, BMI, wrist circumference, wrist width. smoking and handedness as predictors of improvement (or no improvement) in the NeuroQOL and CTSAQ-measured clinical severity scale.
Time frame: 6 weeks
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