Tiny nerve zap study probes migraine pain mystery
NCT ID NCT06022848
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This small study looked at how occipital nerve stimulation (ONS) changes the way people with chronic migraine or cluster headache feel pain. Researchers used special tests and questionnaires to measure pain markers before and after ONS, and compared results to people having non-painful surgery or healthy volunteers. The goal was to understand how ONS affects pain processing, 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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6 people
The number who actually took part.
- Started
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Sep 2019
- Finished
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Jan 2026
- 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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Accepted
You do not need to have the condition being studied to take part.
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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 Subject satisfies standard criteria in the study centre for ONS implantation and the NICE 452 criteria for intractable chronic migraine or cluster headache. Patients who have given their written informed consent. Patient is able and willing to comply with study procedures and follow up schedule. Participants will need a good understanding of the English Language and hence. This is a requirement not just for this research but also for the success of the interventions and the full understanding of QST. Patients undergoing surgery (non-painful complaint) 'dilatation and curettage' (D\&C). Exclusion criteria * Any inclusion criteria not met * Female patients of childbearing age who is or plans on becoming pregnant during the course of the study * Patients with diabetes * Patients known to have a condition that in the investigator's judgment precludes participation in the study. * Patients who have received an investigational drug or have used an investigational device in the 30 days preceding to study entry
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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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Barts health NHS Trust
London, EC1A7BE, United Kingdom
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Other studies related to the condition(s) this trial covers.
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