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Clinical Trial Summary

The purpose of this research study is to assess the long term safety of Dysport® in hemiparetic subjects with upper limb spasticity due to stroke or traumatic brain injury over repeated treatment cycles.


Clinical Trial Description

This was a phase III, multicentre, prospective, open label, repeat treatment cycles, extension to the double study Y-52-52120-145 (Study 145) . The study included both rollover subjects from Study 145 and de novo subjects. The primary study objective was to assess the long term safety of Dysport® in hemiparetic subjects with upper limb spasticity due to stroke or traumatic brain injury over repeated treatment cycles. The secondary study objective was to assess the long term efficacy of repeated treatment with Dysport®. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01313312
Study type Interventional
Source Ipsen
Contact
Status Completed
Phase Phase 3
Start date November 2011
Completion date December 2014

See also
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Completed NCT01313299 - Dysport® Adult Upper Limb Spasticity Phase 3