CD-PROBE: Cervical Dystonia Patient Registry for the Observation of Botulinum Toxin Type A Efficacy
| Status: | Completed |
|---|---|
| Conditions: | Neurology, Orthopedic, Women's Studies |
| Therapuetic Areas: | Neurology, Orthopedics / Podiatry, Reproductive |
| Healthy: | No |
| Age Range: | Any |
| Updated: | 9/23/2012 |
| Start Date: | January 2009 |
| End Date: | February 2013 |
| Contact: | Allergan Inc |
| Email: | clinicaltrials@allergan.com |
This study is an observational trial which will measure the efficacy of botulinum toxin type
A in treating Cervical Dystonia
Inclusion Criteria:
- 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
Exclusion Criteria:
- 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
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