NCT00200122

Restore Claims Characterization Study

• Status: Completed
• Phase: Phase 4
• Study type: Interventional
• Enrollment: 100 (planned)
• Sponsor: MedtronicNeuro · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

The purpose of this study is to characterize the pain coverage capability of the RESTORE spinal cord stimulation (SCS) and assess health outcomes.

Conditions

• Chronic Refractory Pain Associated With Failed Back Surgery Syndrome, Epidural Fibrosis, Peripheral Causalgia, Complex Regional Pain Syndrome

Interventions

Type	Name	Description
DEVICE	Spinal Cord Stimulation

Timeline

• Start date: 2005-01-01
• Completion: 2007-08-01
• First posted: 2005-09-20
• Last updated: 2009-01-21

Locations

8 sites across 1 country: United States