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

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Blepharospasm
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Brief Title

A Retrospective Chart Review of BOTOX® and Xeomin® for the Treatment 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

 Number of Participants With Adverse Events

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

48

Start Date

January 2013

Completion Date

July 2013

Primary Completion Date

July 2013

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 1 year 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

Norway

Location Countries

Norway

Administrative Informations

NCT ID

NCT01814774

Organization ID

TRU2011

Responsible Party

Sponsor

Study Sponsor

Allergan

Study Sponsor

Medical Director, Study Director, Allergan

Verification Date

June 2014