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Identification of Optimal Stimulation Site for Cervical Dystonia Symptoms: An Exploratory Study

NCT01859247 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 8

Last updated 2016-07-28

Study results available
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Summary

The overall objective of this application is to therapeutically target the dysfunctional premotor-motor interaction in dystonia-and to provide a focused treatment of specific anatomical networks in order to reduce side effects and to improve symptom control over conventional therapies.

Conditions

  • Cervical Dystonia
  • Spasmodic Torticollis

Interventions

DEVICE

rTMS

Sponsors & Collaborators

  • Dystonia Coalition

    collaborator OTHER

  • National Institutes of Health (NIH)

    collaborator NIH

  • National Institute of Neurological Disorders and Stroke (NINDS)

    collaborator NIH

  • University Health Network, Toronto

    collaborator OTHER

  • University of New Mexico

    lead OTHER

Principal Investigators

  • Sarah Pirio Richardson, MD · University of New Mexico

  • H.A. Jinnah, MD · Emory University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
100 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-03-31
Primary Completion
2014-06-30
Completion
2014-06-30

Countries

  • United States

Study Locations

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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 NCT01859247 on ClinicalTrials.gov