Spinal Cord Stimulation Research Study
Completed
Conditions studied: Chronic Low Back and Leg Pain
In brief
The purpose of this study is to characterize subjects' response to spinal cord stimulation with postural changes.
Key facts
- Study ID
- NCT00737581
- Run by
- MedtronicNeuro
- People needed
- 20
- Starts
- 2008-08-01
- Expected to finish
- 2009-04-01
- Last updated by the study team
- 2017-02-01
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Be ambulatory
- Be 18 years of age or older
- Have chronic low back pain and/or leg pain due to neuropathic causes
- Be implanted with the Restore or Restore Advanced system for greater than or equal to 3 months
- Be implanted with percutaneous thoracic leads
- Have stable pain control
- Adjust stimulation parameters manually on a regular basis
- Be willing and able to complete protocol requirements
- Be willing and able to provide written informed consent
- Be male or nonpregnant female
You may not qualify if…
- Plan to enroll in another clinical study during participation in this study, or currently enrolled in another clinical study
- Be morbidly obese
- Had pain-related surgery in the previous 12 weeks of enrollment or intend to undergo surgery during the period of the study
Where it is running
- Medical Advanced Pain Specialists (MAPS) — Edina, Minnesota, United States
- Center for Pain Control — Garland, Texas, United States
Full record on ClinicalTrials.gov
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