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Prospective Study of Deep Brain Stimulation with the VERCISE* System for treatment of Dystonia

Recruiting
Conditions
Dystonia
movement disorder
10028037
10009720
Registration Number
NL-OMON52442
Lead Sponsor
Boston Scientific Benelux
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
20
Inclusion Criteria

-Subject meets criteria established in the locally applicable VERCISE System
Directions for Use (DFU) for dystonia
-Subject is at least 7 years old. Parent or guardian consent is required in
patients who are younger than 18 years at the time of consent

Exclusion Criteria

Subject meets any contraindication in the VERCISE System locally applicable
Directions for Use

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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