To Document the Effectiveness of BoNT-A Injection in Adult Subjects With Upper Limb Spasticity Following Stroke

NCT01020500 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 469

Last updated 2020-11-06

No results posted yet for this study

Summary

The purpose of the study is to assess the responder rate as defined by the achievement of the primary goal from the Goal Attainment Scale following one BoNT-A injection cycle in accordance with routine practices.

Conditions

  • Muscle Spasticity

Sponsors & Collaborators

Principal Investigators

  • Ipsen Study Director · Ipsen

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-01-31
Primary Completion
2011-05-31
Completion
2011-05-31

Countries

  • Australia
  • Austria
  • Belgium
  • China
  • Czechia
  • Denmark
  • Finland
  • France
  • Germany
  • Italy
  • Malaysia
  • Mexico
  • Philippines
  • Portugal
  • Russia
  • Singapore
  • South Korea
  • Spain
  • Sweden
  • Taiwan
  • Thailand
  • 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 NCT01020500 on ClinicalTrials.gov