No intervention
OtherNo treatment (intervention) was administered.
NCT Number: NCT02245958
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.
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Notify Me18 year and older
All sexes
Observational
Colonia Roma Z.P., Mexico
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
No treatment (intervention) was administered.
Time frame: 4 Years
Time frame: 4 Years
Time frame: 4 Years
Time frame: 4 Years
Time frame: 4 Years
Allergan
Industry
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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