Evaluation of Clinical Effects for the Treatment of Cervical Dystonia Using Devices Induce the Hanger Reflex
Not Applicable
Suspended
- Conditions
- Cervical Dystonia
- Registration Number
- JPRN-UMIN000021301
- Lead Sponsor
- Kanazawa Neurosurgical Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Suspended
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
Not provided
Exclusion Criteria
(1)Patients who don't have hanger reflex (2)Patients having a unstable disease, and possibility to change medicines during study (3)Patient ruled unfit by a doctor responsible for the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Evaluate changes between Toronto Western Spasmodic Torticollis Rating Scale (TWSTRS) scores before and 3 months after the trial
- Secondary Outcome Measures
Name Time Method