Brain scans may predict back pain treatment success
NCT ID NCT04658628
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether brain scans can help predict which people with chronic low back pain will get good pain relief from spinal cord stimulation (SCS). Researchers will scan the brains of 42 adults before they receive SCS as part of their normal care. They will then check pain levels two weeks after treatment to see if certain brain patterns can forecast who responds best.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 42 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2021
- Expected to finish
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Nov 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Adults recommended to undergo an SCS trial for chronic back with or without leg pain by their pain management physician
- Ages
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21 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Male or female ≥ 21 years of age at time of consent * Subject has been recommended to undergo an SCS trial for chronic back with or without leg pain by their pain management physician * Chronic low back pain as defined by persistent low back pain despite prior treatments that continues for 12 weeks or longer * Subject signs a valid, Institutional Review Board (IRB)-approved informed consent form (ICF) provided Exclusion Criteria: * Subject is a woman who is not using adequate contraception, is pregnant or breastfeeding or intends to become pregnant during the course of the study * Subject has previously undergone a spinal cord stimulation trial or is already implanted with an active implantable device(s) to treat their pain (Implantable Pulse Generators (IPGs), implantable drug pump, etc.) or pacemaker or implantable cardiac defibrillator * Subject is currently abusing alcohol or illicit drugs * Contraindications to MRIs or the need for recurrent body MRIs * Presence of cardiac pacemakers/defibrillators, implanted medication pumps, intra-cardiac lines, any intracranial implants (e.g., aneurysm clip, shunt, cochlear implant, electrodes) or other implanted stimulators
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University of California Los Angeles
RECRUITINGLos Angeles, California, 90067, United States
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