Can a faint zap beat pain? new study puts nerve stimulation to the test
NCT ID NCT07170722
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether very low-level electrical stimulation of nerves near the spine can reduce chronic pain more than a sham (inactive) device. Twenty adults who already have a nerve stimulator implant took part. Each person received both the real low-level stimulation and the sham for 5 days each, without knowing which was which. The goal was to see if the stimulation truly helps with pain, sleep, and mood.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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20 people
The number who actually took part.
- Started
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Sep 2025
- Finished
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Nov 2025
- 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.
- Ages
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18 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adults, age 18 years or older * Implanted with a dorsal root ganglion (DRG) stimulator for chronic neuropathic pain * Have experienced at least 50% reduction in pain for 3 months or longer on standard DRG therapy * Stable pain medication regimen for at least 4 weeks before enrollment * Able and willing to complete electronic diaries and attend study visits Exclusion Criteria: * Active infection or wound complication at the stimulator implant site * Significant psychiatric illness (for example, uncontrolled depression or psychosis) * Planned surgery, device reprogramming, or medication changes during the study period * Currently pregnant or breastfeeding * Occurrence of any adverse event that meets predefined withdrawal criteria during the study (such as intolerable pain or device-related complications)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Neurokirurgiska kliniken. Neuromodulationsenheten
Umeå, Västerbotten County, 90185, Sweden
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