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Clinical Trial Summary

This post-approval study will primarily evaluate the long-term safety of the MedStream Programmable Infusion System when used in combination with Baclofen for the treatment of severe spasticity. A secondary objective, to assess long-term effectiveness, based on the observed scores on the Ashworth Scale (rigidity for the lower extremities) and their Spasm Scores over the 36-month follow-up period will also be described.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01712087
Study type Observational
Source Codman & Shurtleff
Contact
Status Terminated
Phase
Start date October 1, 2012
Completion date December 17, 2017

See also
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