Spinal Cord Stimulation (SCS) for Neuropathic Pain of Back or Lower Extremity
Stopped early · Not applicable
Conditions studied: Intractable Neuropathic Pain, Pain, Back Pain, Lower Extremity Pain
In brief
The primary objective of this study is to compare the efficacy and patient preference for spinal cord stimulation (SCS) using the Precision device with the electrode array placed at T7 versus placement at T8. Eligible patients will have chronic intractable pain in the back or lower extremities and will have independently elected SCS as the next line of therapy. There is some anecdotal evidence that the coverage of the paresthesia resulting from T7 placement is preferable to that obtained by the more commonly used T8 placement but there has been no study to support this observation.
Key facts
- Study ID
- NCT00399841
- Run by
- Boston Scientific Corporation
- People needed
- 13
- Starts
- 2006-11-01
- Expected to finish
- 2008-11-01
- Last updated by the study team
- 2020-12-19
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Be diagnosed with chronic intractable neuropathic pain of moderate to severe intensity of the back or lower extremity and meeting the criteria for post-laminectomy syndrome, be eligible for SCS, and have independently elected SCS as next line of therapy.
- Be 18 years of age or older.
- Be willing and able to comply with all study related procedures and visits.
- Be capable of reading and understanding patient information materials and giving written informed consent.
You may not qualify if…
- Have sensory loss in the low back or lower extremity as the primary complaint.
- Have any significant medical condition that is likely to interfere with study procedures or likely to confound evaluation of study endpoints.
- Have participated in any investigational drug or device trial in the last 4 weeks or plan to participate in any other study during the year.
Where it is running
- Anesthesia Associates of Belleville — Belleville, Illinois, United States
Full record on ClinicalTrials.gov
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