CD-PROBE: Cervical Dystonia Patient Registry for the Observation of onabotulinumtoxinA Efficacy

Completed

Conditions studied: Cervical Dystonia

In brief

This study is an observational trial which will measure the efficacy of onabotulinumtoxinA in treating Cervical Dystonia.

Key facts

Study ID

NCT00836017

Run by

Allergan

People needed

1046

Starts

2009-01-01

Expected to finish

2013-08-01

Last updated by the study team

2014-07-17

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Diagnosed with Cervical Dystonia
• Candidate for botulinum toxin type A therapy
• New to physician's practice, and/or new to botulinum toxin type A therapy, or has not been injected with botulinum toxin type A for at least 16 weeks as a participant in another clinical trial investigating botulinum toxin type A for cervical dystonia
• Able to follow study instructions and complete study activities

You may not qualify if…

• Patients undergoing elective surgery during the trial period
• Females who are pregnant, nursing, or planning a pregnancy
• History of poor cooperation or compliance with medical treatment or unreliability
• Any condition or situation in which, in the investigator's opinion, places the patient at significant risk, could confound the study data, or may interfere with the patient's participation in the study, including but not limited to unstable medical conditions

Where it is running

• Study site — Springfield, Massachusetts, United States

Full record on ClinicalTrials.gov

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