The purpose of this clinical study is to verify the long term effectiveness and safety of a bilateral deep brain stimulation (DBS) produced by Beijing PINS Medical Co., Ltd. as a treatment option for patients with cognitive, behavioral, and functional disability of Tourette Syndrome.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
20
Modified Rush Video Rating Scale (mRVRS)
Time frame: 12 month
Tourette Syndrome Symptom List (TSSL)
Time frame: 12 month
SF-36
Time frame: 12 month
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