NCT00773019 - SynchroMed II Post-Approval Study | Biotech Hunter

Enrollment

Participants

Timeline

Start Date

November 30, 2004

Primary Completion Date

June 30, 2008

Study Completion Date

November 30, 2008

Conditions

Severe SpasticityChronic Pain

Interventions

DEVICE

Refills (SynchroMed® II Programmable Drug Infusion Pump)

Refill information at 1, 6, and 12 months post-implant, as well as any additional refills required from implant through end of study. Amount removed from the pump (taken from syringe), Amount placed in the pump (from syringe),Pump predicted amount remaining in the pump.