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Spinal Cord Stimulation Research Study

Posture Responsive Spinal Cord Stimulation Research Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00737581
Enrollment
20
Registered
2008-08-19
Start date
2008-08-31
Completion date
2009-04-30
Last updated
2017-02-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Low Back and Leg Pain

Keywords

Subject's, response, changes, in spinal, cord, stimulation, during, postural

Brief summary

The purpose of this study is to characterize subjects' response to spinal cord stimulation with postural changes.

Interventions

None listed

Sponsors

MedtronicNeuro
Lead SponsorINDUSTRY

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 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

Exclusion criteria

* 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

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026