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OpenTrials
Completed

NCT Number: NCT00737581

Spinal Cord Stimulation Research Study

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

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Medical Advanced Pain Specialists (MAPS), Edina, Minnesota, United States

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Sponsors and collaborators

Lead sponsor

MedtronicNeuro

Industry

Registry information

Official study title

Posture Responsive Spinal Cord Stimulation Research Study

Important dates

Study start
2008
Primary completion
2009
Study completion
2009
First posted
Aug 19, 2008
Registry last updated
Feb 1, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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