DYSPORT™ Clinical & Health Economics Outcomes Registry in Cervical Dystonia

NCT01314365 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 350

Last updated 2020-11-05

No results posted yet for this study

Summary

The purpose of the protocol is to determine typical patient response to Dysport in the treatment of adult cervical dystonia (CD).

Conditions

  • Cervical Dystonia

Sponsors & Collaborators

Principal Investigators

  • Ipsen Study Director · Ipsen

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-04-30
Primary Completion
2013-11-30
Completion
2014-03-31

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01314365 on ClinicalTrials.gov