Tourette Syndrome Clinical Trial
Official title:
The Safety and Efficacy of Long-term Treatment of PINS Stimulator System for Tourette Syndrome
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.
Status | Not yet recruiting |
Enrollment | 20 |
Est. completion date | December 2018 |
Est. primary completion date | December 2018 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: 1. Subject is aged 18 or older 2. Patient Group with Tourette's syndrome, Diagnosis of Tourette Syndrome by DSM-IV Exclusion Criteria: 1. Major Depressive Episode within the previous 6 months 2. Schizophrenia or other psychotic disorder.Participate in other clinical trial; 3. Has a life expectancy of < 1 year. 4. The investigator and/or enrollment review committee, would preclude participation in the study. |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Beijing Pins Medical Co., Ltd | Beijing Tiantan Hospital |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Modified Rush Video Rating Scale (mRVRS) | 12 month | Yes | |
Secondary | Tourette Syndrome Symptom List (TSSL) | 12 month | Yes | |
Secondary | SF-36 | 12 month | Yes |
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