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Trial record 24 of 116 for:    cervical | "dopa-responsive dystonia" OR "Dystonia"

Integration of the Cervical Proprioceptive Signals in Patients With Cervical Dystonia (STAC2)

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ClinicalTrials.gov Identifier: NCT02834871
Recruitment Status : Completed
First Posted : July 15, 2016
Last Update Posted : March 28, 2017
Sponsor:
Information provided by (Responsible Party):
Fondation Ophtalmologique Adolphe de Rothschild

Brief Summary:
The purpose of this study is to compare the cervical muscular force control , taking into account the proprioceptive signals, in patients with and without cervical dystonia.

Condition or disease Intervention/treatment Phase
Cervical Dystonia Device: Electromyogram Not Applicable

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 40 participants
Allocation: Non-Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Basic Science
Actual Study Start Date : March 2015
Actual Primary Completion Date : July 2015
Actual Study Completion Date : July 2015


Arm Intervention/treatment
patients with cervical dystonia
Computerized assessment of the cervical muscular force and with electromyogram in patients with cervical dystonia
Device: Electromyogram
patients without cervical dystonia
Computerized assessment of the cervical muscular force and with electromyogram in patients without cervical dystonia
Device: Electromyogram



Primary Outcome Measures :
  1. Measuring (in Newton) of the muscular force exerted by extending movements of the cervical spine in static and dynamic condition [ Time Frame: two hours ]


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Ages Eligible for Study:   18 Years to 70 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion criteria:

  • patients presenting focal or segmental cervical dystonia diagnosed by a neurologist expert in the diseases with abnormal movements
  • having signed a consent for study participation

No Inclusion Criteria:

Neurological affection other than cervical dystonia (typical or atypical parkinsonism, other ...)

  • Severe pain, trauma or disease of the cervical spine known or suspected other than cervical dystonia requiring treatment in the last 6 months
  • Ongoing neuroleptic treatment
  • Pregnancy or breastfeeding
  • Lack of insurance coverage

For patients, are added the following no inclusion criteria are added:

  • Trembling cervical dystonia
  • Injection of botulinum toxin in the past three months

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02834871


Locations
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France
Fondation Ophtalmique Adolphe de Rothschild
Paris, France, 75019
Sponsors and Collaborators
Fondation Ophtalmologique Adolphe de Rothschild

Publications of Results:
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Responsible Party: Fondation Ophtalmologique Adolphe de Rothschild
ClinicalTrials.gov Identifier: NCT02834871     History of Changes
Other Study ID Numbers: SSA_2014_23
First Posted: July 15, 2016    Key Record Dates
Last Update Posted: March 28, 2017
Last Verified: March 2017

Additional relevant MeSH terms:
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Dystonia
Dystonic Disorders
Torticollis
Dyskinesias
Neurologic Manifestations
Nervous System Diseases
Signs and Symptoms
Movement Disorders
Central Nervous System Diseases