Long-term Surveillance of the MedStream Programmable Infusion System

Status Terminated

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

Clinical Trial Details

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

View Details

See also
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