Efficacy and Safety of Deep Brain Stimulation (DBS) of the Pallidal (GPi) in Patients With Tardive Dystonia
NCT00331669 · Status: UNKNOWN · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 24
Last updated 2009-03-04
Summary
The purpose of this randomized, double blind, multi-center study is to assess the efficacy and safety of bilateral pallidal deep brain stimulation in patients with tardive dystonia.
Conditions
- Dystonia
- Movement Disorder
Interventions
- PROCEDURE
-
deep brain stimulation
high frequency stimulation
Sponsors & Collaborators
-
Humboldt-Universität zu Berlin
collaborator OTHER -
Ruhr University of Bochum
collaborator OTHER -
Medical University of Cologne
collaborator OTHER -
Heinrich-Heine University, Duesseldorf
collaborator OTHER -
University Hospital Freiburg
collaborator OTHER -
Medical University of Hannover
collaborator OTHER -
Medical University Innsbruck
collaborator OTHER -
University of Kiel
collaborator OTHER -
Philipps University Marburg
collaborator OTHER -
Ludwig-Maximilians - University of Munich
collaborator OTHER -
University of Rostock
collaborator OTHER -
University of Regensburg
collaborator OTHER -
University Hospital Tuebingen
collaborator OTHER -
Medical University of Vienna
collaborator OTHER - collaborator INDUSTRY
-
Charite University, Berlin, Germany
lead OTHER
Principal Investigators
-
Andreas R Kupsch, MD · Dpt. of Neurology, Augustenburger Platz 1, 13353 Berlin, Charite, Campus Virchow, Germany
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- TRIPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 75 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2006-05-31
- Completion
- 2010-12-31
Countries
- Germany
Study Locations
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