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NCT06023953Completed

Migraine With and Without Aura Characteristics and Response to Remote Electrical Neuromodulation (REN) Treatment

Comparison of Migraine With and Without Aura in a Large Cohort: Characteristics and Response to Remote Electrical Neuromodulation (REN) Treatment

Source: ClinicalTrials.gov · Last updated 15 Aug 2025

Brief summary (registry, in English)

This is a Post-marketing, real-world evidence study investigating the safety and efficacy of the acute treatment of migraine with a Remote Electrical Neuromodulation (REN) device (Nerivio) in migraine patients with and without aura, as well as characterizing demographic and attack characteristic differences between migraine patients with and without aura. Safety will be assessed by the number and type of device-related adverse events. Efficacy will be evaluated as a change in headache pain severity from baseline to 2 hours post-treatment. Disease characteristics will look into demographic and attack differences between patients with and without aura.

Status (registry)
Completed
Study type
Observational
Enrollment
31715 (actual)
First submitted
29 Aug 2023
Start date
1 Jul 2023
Primary completion date
30 Sept 2024
Lead sponsor
Theranica
Diseases
Migraine
NCT number
NCT06023953

What you commit to

  • Study type: Observational
  • Participants enrolled: 31715
  • From 1 Jul 2023 to the primary completion date, 30 Sept 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Users who prospectively reported having aura only once

Who the study is looking for

  • Users aged 8 years old and above
  • Users who treated their migraine attacks with the Nerivio device at least twice
  • Users who prospectively reported the presence of aura in at least two treatment reports (reporting at least twice having aura) , OR:
  • Users who prospectively reported the absence of aura in all of their reports, with at least two reports

Age in the registry: 8 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Theranica Bio-Electronics Ltd
Coordinator of this site? Confirm its status
NetanyaIsraelUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.