Factors Influencing Response to One BoNT-A Injection Cycle in Subjects Suffering From Idiopathic Cervical Dystonia

NCT00833196 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 404

Last updated 2019-08-16

No results posted yet for this study

Summary

A post marketing, international, multicenter, observational, prospective, longitudinal study. The purpose of the study is to describe cervical dystonia sub-types with their injection protocols and response to BoNT-A.

Conditions

  • Idiopathic Cervical Dystonia

Sponsors & Collaborators

Principal Investigators

  • Ipsen Medical Director · Ipsen

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-02-28
Primary Completion
2010-02-28
Completion
2010-04-30

Countries

  • Australia
  • Belgium
  • Czechia
  • France
  • Germany
  • Netherlands
  • Portugal
  • Russia
  • United Kingdom

Study Locations

More Related Trials

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 NCT00833196 on ClinicalTrials.gov