Carpal tunnel syndrome
Conditions
Interventions
Normal subjects group versus CTS group:Surgery: median nerve release
Sponsors
Shanghai Jin'an District Central Hospital
Eligibility
Sex/Gender
All
Age
40 Years to 65 Years
Inclusion criteria
Inclusion criteria: Patient group access criteria: (1) clinically diagnosed patients with carpal tunnel syndrome; (2) intelligence, language and visual and auditory function is normal; (3) age is not limited, men and women are not limited; 40-65 year old women priority included (4) right hand (5) Patient him/herself desired to improve the hand discomfort by surgery; (6) willing to accept including clinical physical examination, EEG, EMG and magnetic resonance examination, follow follow-up arrangements Control group selection criteria: (1) healthy people; (2) intelligence, language and visual and auditory function is normal; (3) Any age men and women; age and sex matched with experimental group; (4) right hand; (5) willing to accept including clinical physical examination, EEG, EMG and magnetic resonance examination, follow follow-up arrangements.
Exclusion criteria
Exclusion criteria: Patient group exclusion criteria: (1) have the following diseases: diabetes, cervical spondylosis, rheumatism and rheumatoid arthritis, peripheral neuritis, wrist trauma, chronic pain, depression and other mental illness or disorder, cerebrovascular disease, brain trauma, Kindergarten, Alzheimer's disease, multiple sclerosis, severe systemic disease; (2) the presence of metal implants, pacemakers, tattoos; (3) to participate in this study before any form of treatment (including other diseases), such as physical therapy, taking drugs; (4) no intention of surgical treatment; (5) can not follow the follow-up arrangements; Control group exclusion criteria: (1) have the following diseases: diabetes, cervical spondylosis, rheumatism and rheumatoid arthritis, peripheral neuritis, wrist trauma, chronic pain, depression and other mental illness or disorder, cerebrovascular disease, brain trauma, Kindergarten, Alzheimer's disease, multiple sclerosis, severe systemic disease. (2) the presence of metal implants, pacemakers, tattoos; (3) to participate in this study before any form of treatment or medication history; (4) can not follow the follow-up arrangements.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| fMRI:Activation; | — |
Secondary
| Measure | Time frame |
|---|---|
| fMRI:Diffusion Tensor Imaging;fMRI:Functional Connectivity;fMRI:Resting-State;EEG; | — |
Countries
China
Contacts
Public ContactWendong Xu
Department of Hand Surgery, Huashan Hospital, Fudan University
Outcome results
None listed