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Clinical Trials/NCT02834871
NCT02834871CompletedNot Applicable

Integration of the Cervical Proprioceptive Signals in Patients With Cervical Dystonia

Fondation Ophtalmologique Adolphe de Rothschild2 sites in 1 country40 target enrollmentStarted: March 2015Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
40
Locations
2
Primary Endpoint
Measuring (in Newton) of the muscular force exerted by extending movements of the cervical spine in static and dynamic condition

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Basic Science
Masking
None

Eligibility Criteria

Ages
18 Years to 70 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
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

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Measuring (in Newton) of the muscular force exerted by extending movements of the cervical spine in static and dynamic condition

Time Frame: two hours

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Network
Responsible Party
Sponsor

Study Sites (2)

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