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A Prospective Clinical Outcomes Registry — PAIN Registry  

Pain Clinical Trial

Official title:
Partnership for Advancement In Neuromodulation (PAIN): A Prospective Clinical Outcomes Registry

Clinical Trial Summary

This is a prospective non-interventional 24 month post implant registry. Any patient that receives a St. Jude Medical FDA approved implantable neuromodulation system is eligible for enrollment. A minimum of 600 patients will be enrolled from a minimum of 30 sites.

Patients will be enrolled post-implant and followed for 24 months. Data are collected at enrollment (within 30 days of device implant), and routine care follow-up visits at 3 months, 6 months, 12 months, 18 months and 24 months.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01305525
Study type Observational
Source Abbott Medical Devices
Contact
Status Completed
Phase
Start date June 2009
Completion date April 2014
View Details
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