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Double-blind, Multicenter Study to Assess the Efficacy of Bilateral Pallidal Stimulation in Patients With Medically Refractory Primary Cervical Dystonia

NCT00148889 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 63

Last updated 2018-02-19

No results posted yet for this study

Summary

The purpose of this study is to investigate the efficacy and safety of bilateral pallidal stimulation in patients with medically refractory primary cervical dystonia.

Conditions

  • Cervical Dystonia

Interventions

DEVICE

Deep brain stimulation (DBS)

Bilateral pallidal stimulation with an implanted DBS device

Sponsors & Collaborators

  • Medtronic

    collaborator INDUSTRY

  • Competence Network on Parkinson's Disease

    collaborator OTHER

  • German Parkinson Study Group (GPS)

    lead OTHER

Principal Investigators

  • Joerg Mueller, MD · Department of Neurology, Medical University Innsbruck, Anichstr. 35, A-6020 Innsbruck, Austria

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-07-31
Primary Completion
2008-04-30
Completion
2008-04-30

Countries

  • Austria
  • Germany

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00148889 on ClinicalTrials.gov