A Retrospective Chart Review of BOTOX® and Xeomin® for the Management of Cervical Dystonia and Blepharospasm

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Brief Title

A Retrospective Chart Review of BOTOX® and Xeomin® for the Management of Cervical Dystonia and Blepharospasm


Brief Summary

      This study is a retrospective chart review to evaluate the doses of botulinum Type A toxins
      BOTOX® (onabotulinumtoxinA) and Xeomin® (incobotulinumtoxinA) used for the treatment of
      Cervical Dystonia and Blepharospasm in clinical practice.
    



Study Type

Observational


Primary Outcome

Dose of Botulinum Toxin Used to Treat Cervical Dystonia

Secondary Outcome

 Botulinum Toxin Inter-injection Intervals

Condition

Cervical Dystonia

Intervention

No Intervention

Study Arms / Comparison Groups

 BOTOX®
Description:  Retrospective chart review of doses of BOTOX® (onabotulinumtoxinA) used as standard of care in clinical practice. No treatment (intervention) was administered.

Publications

* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.

Recruitment Information


Recruitment Status

Other

Estimated Enrollment

44

Start Date

August 2015

Completion Date

December 2015

Primary Completion Date

December 2015

Eligibility Criteria

        Inclusion Criteria:

          -  Confirmed primary diagnosis of idiopathic cervical dystonia or blepharospasm for at
             least 2 years

          -  Treatment with Xeomin® and BOTOX® for at least 2 years each.

        Exclusion Criteria:

          -  Having a neuromuscular junction transmission disorder or taking any medications that
             could affect neuromuscular junction transmission

          -  Previous surgical procedure involving bone or muscle for the management of cervical
             dystonia or blepharospasm.
      

Gender

All

Ages

18 Years - N/A

Accepts Healthy Volunteers

No

Contacts

Medical Director, , 

Location Countries

Mexico

Location Countries

Mexico

Administrative Informations


NCT ID

NCT02245958

Organization ID

GMA-US-NEU-0271


Responsible Party

Sponsor

Study Sponsor

Allergan


Study Sponsor

Medical Director, Study Director, Allergan


Verification Date

January 2016