TerminatedNot Applicable

Change in Pain and Quality of Life Following SCS for Chronic Pain

Stopped: Sponsor withdrew funding

United States26 participantsStarted 2017-11-01

Plain-language summary

Study Title Subject-reported treatment efficacy and procedure satisfaction (steps) study.BURST study- a prospective observational clinical study examining the changes in quality of life and pain following spinal cord stimulation for the treatment of chronic intractable lower back and lower limb pain.

Who can participate

Age range18 Years – 85 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: Prescribed spinal cord stimulator implant by their healthcare provider. Previous conservative care such as physical therapy or chiropractic care that failed to provide adequate pain relief. Willing and able to adhere to the protocol of the study including the survey timeline. Between the ages of 18-85 years. Exclusion Criteria: Unwilling to sign Informed Consent and comply with protocol

What they're measuring

Change in Pain Levels

Timeframe: 12 months post-permanent spinal cord stimulator implantation

Change in quality of life

Timeframe: 12 months post-permanent spinal cord stimulator implantation

Trial details

NCT IDNCT03421951

SponsorKM Clinical Research Group

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2019-01-31

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