Viewing Study NCT00370695



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Last Modification Date: 2024-10-26 @ 9:27 AM
Study NCT ID: NCT00370695
Status: TERMINATED
Last Update Posted: 2020-12-17
First Post: 2006-08-30

Brief Title: Spinal Cord Stimulation for Chronic and Intractable Back Pain
Sponsor: Boston Scientific Corporation
Organization: Boston Scientific Corporation

Study Overview

Official Title: Spinal Cord Stimulation for Chronic and Intractable Back Pain in Patients Who Are Not Surgical Candidates
Status: TERMINATED
Status Verified Date: 2020-11
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Insufficient Data Collected
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to evaluate the efficacy of spinal cord stimulation SCS using the Precision implantable neurostimulation device for chronic and intractable back pain in subjects who are not candidates for surgery or who have chosen to seek alternative therapy
Detailed Description: Management of symptoms of chronic back pain andor lumbar radiculopathy is often difficult and inadequate Current treatment options include pharmacological treatments physical therapy nerve blocks surgical interruption of the pain pathway or back surgery Many patients either do not have adequate pain management with conventional treatments or are not able to tolerate the treatments due to significant side effects Similarly many patients are either not candidates for surgical interventions or are unwilling to undergo such procedures Spinal cord stimulation has proven to be an effective treatment for patients with pain following a failed back surgery and this study will investigate spinal cord stimulation as a treatment option for the treatment of chronic back pain in patients who have never had back surgery A successful study outcome will establish spinal cord stimulation as a less-invasive treatment option to be considered prior to surgery

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None