Brain zapping study reveals how pain relief works
NCT ID NCT02849834
First seen Jun 27, 2026 ยท Last updated Jun 27, 2026
Summary
This study looked at how a non-invasive magnetic brain stimulation technique called rTMS changes brain activity in healthy volunteers and people with long-term nerve pain. Researchers measured brain responses before and after stimulation to see if these changes relate to pain relief. The goal was to better understand how rTMS works, not to test a new treatment.
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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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65 people
The number who actually took part.
- Start date
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Nov 2009
- Finished
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Nov 2016
- 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 to 70 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * healthy subjects aged from 18 to 70 years, male or female, with social protection, fully informed and having given their written consent. * patients : * aged from 18 to 80 years, male or female, with social protection , fully informed and having given their written consent. * unilateral pharmacoresistant neuropathic pain during at least one year, * without any change of the pharmacological treatment since at least one month Exclusion Criteria: * for healthy subjects only: * history of chronic pain * analgesic medication within 24h before stimulation For patients only: new analgesic treatment within 1 month before consent for both: * drug addiction, headache, epilepsy history * ferromagnetic intracranial device * implanted stimulator * absence of contraceptive method for women of childbearing age
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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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Service d'Exploration, Centre Hospitalier Lyon Est, Hospices civils de Lyon, Lyon, F-69495, France et NeuroPain lab - CRNL (Inserm U1028 - UCBL)
Bron, 69500, France
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Other studies related to the condition(s) this trial covers.
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